NP-MRD: Showing NP-Card for 2,5-Dimethoxy-3-undecylphenol. (NP0086440)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 06:44:38 UTC

Updated at

2022-04-29 06:44:38 UTC

NP-MRD ID

NP0086440

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,5-Dimethoxy-3-undecylphenol.

Description

2,5-Dimethoxy-3-undecylphenol belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. 2,5-Dimethoxy-3-undecylphenol. is found in Averrhoa carambola . Based on a literature review very few articles have been published on 2,5-dimethoxy-3-undecylphenol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 54  0  0  0  0  0  0  0  0999 V2000
    5.3539    3.0018   -0.3165 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2950    2.0533   -1.4676 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0406    0.6449   -1.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7685    0.2364   -0.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3888    0.8773    0.7989 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0684    0.2913    1.3252 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2325   -1.1555    1.6404 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9840   -1.7846    2.1760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1163   -1.7655    1.1463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3694   -2.3525    1.7369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4759   -2.3873    0.7670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9355   -1.0978    0.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6018    0.1119    0.7664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0550    1.3227    0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6740    2.5215    0.8556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1337    3.7454    0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8800    1.3349   -0.8475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2203    0.1157   -1.3979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0638    0.1712   -2.5190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7802   -1.0782   -0.9041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1164   -2.3130   -1.4507 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2523   -3.0421   -0.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5194    2.5235    0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4436    3.6186   -0.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2624    3.6721   -0.4762 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5386    2.4703   -2.1881 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2652    2.0579   -2.0501 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2585    0.0191   -2.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8730    0.3545   -0.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9450    0.3552   -1.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8204   -0.8938   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1326    0.6656    1.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2618    1.9791    0.7255 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3176    0.4308    0.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7610    0.8947    2.2100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0482   -1.2931    2.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5689   -1.7611    0.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5967   -1.2744    3.0795 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2292   -2.8419    2.4347 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1826   -2.5167    0.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2048   -0.8206    0.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0758   -3.3985    2.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6406   -1.8497    2.6945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3586   -2.8828    1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2717   -3.0857   -0.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9710    0.1632    1.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9149    3.7716   -0.7607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2303    3.8667    0.4357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6565    4.5770    0.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2550    2.2809   -1.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3222   -0.7133   -2.9292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0177   -3.0564   -1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9392   -4.1130   -0.8122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6236   -2.6514   -0.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 20 12  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  0
 11 45  1  0
 13 46  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  0
 19 51  1  0
 22 52  1  0
 22 53  1  0
 22 54  1  0
M  END


  Mrv1652304292208442D          

 22 22  0  0  0  0            999 V2000
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086440

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC1=CC(OC)=CC(O)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C19H32O3/c1-4-5-6-7-8-9-10-11-12-13-16-14-17(21-2)15-18(20)19(16)22-3/h14-15,20H,4-13H2,1-3H3

> <INCHI_KEY>
IXMXPKGDLIPGOO-UHFFFAOYSA-N

> <FORMULA>
C19H32O3

> <MOLECULAR_WEIGHT>
308.462

> <EXACT_MASS>
308.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.53187735329946

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,5-dimethoxy-3-undecylphenol

> <ALOGPS_LOGP>
6.40

> <JCHEM_LOGP>
6.313446002333333

> <ALOGPS_LOGS>
-5.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.013175799721859

> <JCHEM_PKA_STRONGEST_BASIC>
-4.546950917557648

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
92.01649999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.11e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,5-dimethoxy-3-undecylphenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.337 -12.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.005 -11.550   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.339 -12.320   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      22.673 -11.550   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      22.673 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      20.005 -16.170   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      17.338 -14.630   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      16.004 -13.860   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   12   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₃₂O₃

Average Mass

308.4620 Da

Monoisotopic Mass

308.23514 Da

IUPAC Name

2,5-dimethoxy-3-undecylphenol

Traditional Name

2,5-dimethoxy-3-undecylphenol

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC1=CC(OC)=CC(O)=C1OC

InChI Identifier

InChI=1S/C19H32O3/c1-4-5-6-7-8-9-10-11-12-13-16-14-17(21-2)15-18(20)19(16)22-3/h14-15,20H,4-13H2,1-3H3

InChI Key

IXMXPKGDLIPGOO-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Averrhoa carambola	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

P-dimethoxybenzene
Dimethoxybenzene
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Monocyclic benzene moiety
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	6.4	ALOGPS
logP	6.31	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	10.01	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	92.02 m³·mol⁻¹	ChemAxon
Polarizability	38.53 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	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

C00056713

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

89782462

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2,5-Dimethoxy-3-undecylphenol. (NP0086440)

MOL for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

3D MOL for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

3D SDF for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

3D-SDF for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

PDB for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

3D PDB for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

SMILES for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

INCHI for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

Structure for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)

3D Structure for NP0086440 (2,5-Dimethoxy-3-undecylphenol.)