NP-MRD: Showing NP-Card for 6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran (NP0198131)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 16:31:15 UTC

Updated at

2022-09-04 16:31:15 UTC

NP-MRD ID

NP0198131

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran

Description

6-[(3,7-Dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-1,3-dihydro-2-benzofuran belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Based on a literature review very few articles have been published on 6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-1,3-dihydro-2-benzofuran.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042218312D          

 28 29  0  0  0  0            999 V2000
    2.5645    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5658   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726   -0.8134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9429   -1.0637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7248   -1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  6 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 62 63  0  0  0  0  0  0  0  0999 V2000
   -4.2870   -1.2041    3.6382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1808    0.0641    3.0131 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4018    0.1608    1.8678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0620    0.4629    2.0312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4568    0.6802    3.3746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2880    0.5586    0.8868 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0525    0.8623    1.0744 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9097    0.9778   -0.0451 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2898    1.3023    0.3334 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3677    0.5443    0.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1100   -0.7077   -0.6682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6909    0.9766    0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7156    1.2386   -0.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0443    0.0880   -1.3850 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2577   -0.4381   -1.4115 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3133    0.1522   -0.5479 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5774   -1.6005   -2.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8172    0.3624   -0.3846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1333    0.0665   -0.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9131   -0.0311    0.6019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2779   -0.3594    0.1149 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1904    0.6392    0.3413 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2067    0.2603    1.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1574   -0.7596   -1.1900 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9982   -0.1969   -1.7065 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3370   -1.2522   -2.5680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3095    0.9458   -2.4043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1788    0.5788   -3.4405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1018   -1.1213    4.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3322   -1.6011    3.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6277   -1.9638    3.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1958    0.4923    4.1544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1155    1.7391    3.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5560    0.0393    3.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182    1.8825   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654    0.1299   -0.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5015    2.2369    0.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1887   -1.1723   -0.2103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9319   -0.5708   -1.7478 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8981   -1.4783   -0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1543    0.2235    1.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6181    1.9085    1.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4940    2.1589   -1.1258 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6593    1.5135    0.0345 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2854   -0.3324   -2.0216 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2582   -0.3794   -0.7220 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0075    0.0656    0.5158 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4757    1.2177   -0.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4690   -2.1556   -1.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7439   -2.3402   -2.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7950   -1.2381   -3.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751    0.4470   -1.2512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6059   -1.2518    0.7177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7161   -0.6198    0.7239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8112   -0.0841    2.1720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9894    1.0360    1.2885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0646   -1.8917   -3.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6153   -0.7813   -3.2734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7091   -1.9205   -1.9190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6772   -0.1569   -4.1039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1268    0.1640   -3.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4770    1.4327   -4.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  6
 27 28  1  0
 25 19  1  0
 19 20  2  0
 20  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  3
 15 16  1  0
 15 17  1  0
  6 18  2  0
 20 21  1  0
 18 19  1  0
 23 54  1  0
 23 55  1  0
 23 56  1  0
 21 53  1  1
 26 57  1  0
 26 58  1  0
 26 59  1  0
 28 60  1  0
 28 61  1  0
 28 62  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  5 32  1  0
  5 33  1  0
  5 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
 11 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
M  END


  Mrv1652309042218312D          

 28 29  0  0  0  0            999 V2000
    2.5645    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5658   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726   -0.8134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9429   -1.0637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7248   -1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  6 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198131

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1OC(C)(OC)C2=C1C(OC)=C(C)C(OCC=C(C)CCC=C(C)C)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O5/c1-15(2)10-9-11-16(3)12-13-27-19-14-18-20(21(24-6)17(19)4)22(25-7)28-23(18,5)26-8/h10,12,14,22H,9,11,13H2,1-8H3

> <INCHI_KEY>
NUMMDABPEFZWBV-UHFFFAOYSA-N

> <FORMULA>
C23H34O5

> <MOLECULAR_WEIGHT>
390.52

> <EXACT_MASS>
390.240624195

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.59730244568823

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-1,3-dihydro-2-benzofuran

> <JCHEM_LOGP>
5.625156926000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8360478904229827

> <JCHEM_POLAR_SURFACE_AREA>
46.150000000000006

> <JCHEM_REFRACTIVITY>
113.65210000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3H-2-benzofuran

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.787   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.121   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.788   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.788  -0.770   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.788  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.122  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.122  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.788  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.455  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.455  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.789  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.789  -9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.123 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.455 -10.010   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.846   3.481   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.340   3.801   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.417   0.770   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.189  -1.518   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.627  -1.986   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.086  -2.477   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18    6   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19    3   21                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24   19   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₄O₅

Average Mass

390.5200 Da

Monoisotopic Mass

390.24062 Da

IUPAC Name

6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-1,3-dihydro-2-benzofuran

Traditional Name

6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3H-2-benzofuran

CAS Registry Number

Not Available

SMILES

COC1OC(C)(OC)C2=C1C(OC)=C(C)C(OCC=C(C)CCC=C(C)C)=C2

InChI Identifier

InChI=1S/C23H34O5/c1-15(2)10-9-11-16(3)12-13-27-19-14-18-20(21(24-6)17(19)4)22(25-7)28-23(18,5)26-8/h10,12,14,22H,9,11,13H2,1-8H3

InChI Key

NUMMDABPEFZWBV-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Bicyclic monoterpenoid
Aromatic monoterpenoid
Isocoumaran
Anisole
Ketal
Alkyl aryl ether
Benzenoid
Oxacycle
Organoheterocyclic compound
Ether
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.63	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	46.15 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	113.65 m³·mol⁻¹	ChemAxon
Polarizability	45.6 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

78141416

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran (NP0198131)

MOL for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

3D MOL for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

3D SDF for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

3D-SDF for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

PDB for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

3D PDB for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

SMILES for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

INCHI for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

Structure for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)

3D Structure for NP0198131 (6-[(3,7-dimethylocta-2,6-dien-1-yl)oxy]-1,3,4-trimethoxy-1,5-dimethyl-3h-2-benzofuran)