NP-MRD: Showing NP-Card for 3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol (NP0227866)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 07:20:18 UTC

Updated at

2022-09-06 07:20:18 UTC

NP-MRD ID

NP0227866

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol

Description

Alpha,alpha,6-Trimethyl-4-(3-hydroxy-5-methylphenoxy)-2,3-dihydrobenzofuran-2beta-methanol belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups. Based on a literature review very few articles have been published on alpha,alpha,6-Trimethyl-4-(3-hydroxy-5-methylphenoxy)-2,3-dihydrobenzofuran-2beta-methanol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
   -5.5263    0.3127   -1.9258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6650    0.5100   -0.7388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2486    0.5933    0.5214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4933    0.7753    1.6484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1193    0.8522    2.8814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1321    0.8789    1.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5321    0.7975    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1604    0.8988    0.1542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3651   -0.2399    0.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9474   -1.4658    0.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1583   -2.5782    0.4553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7936   -3.9228    0.6639 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2124   -2.5103    0.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8122   -1.2595    0.1292 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0055   -0.1458    0.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9004    1.0489   -0.1355 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2116    0.4800    0.3345 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4139    1.1315   -0.2948 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5873    2.5597    0.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6259    0.2842    0.1133 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3515    1.0629   -1.6853 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1346   -0.8801   -0.0331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3033    0.6137   -0.8421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9223   -0.1765   -2.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3885   -0.3597   -1.7181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8610    1.3117   -2.2771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3293    0.5126    0.6189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4267    1.7343    3.2560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4864    1.0234    2.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007   -1.5734    0.5081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8723   -3.8699    0.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7023   -4.1910    1.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2555   -4.6730    0.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8322   -3.3955    0.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8878    1.3501   -1.1808 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5730    1.8520    0.5563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2325    0.5274    1.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6808    2.8071   -0.0406 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3213    2.7506    1.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0474    3.2219   -0.6151 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5672    0.7198   -0.2203 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5514    0.1047    1.2007 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4607   -0.7132   -0.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1549    0.6950   -2.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8750    0.5447   -1.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 22  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 15  9  1  0
  9  8  1  0
  8  7  1  0
  7 23  2  0
 23  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  9 10  2  0
 10 11  1  0
 22 14  1  0
  6  7  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 16 35  1  0
 16 36  1  0
 17 37  1  1
 19 38  1  0
 19 39  1  0
 19 40  1  0
 20 41  1  0
 20 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  5 28  1  0
  6 29  1  0
 10 30  1  0
M  END


  Mrv1652309062209202D          

 23 25  0  0  1  0            999 V2000
    4.7079    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    3.3000    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
    6.1368    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    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
    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 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
    1.2949    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3551    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  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  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 17 22  1  0  0  0  0
 14 22  1  0  0  0  0
  7 23  2  0  0  0  0
  2 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0227866

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC2=C(C[C@@H](O2)C(C)(C)O)C(OC2=CC(C)=CC(O)=C2)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H22O4/c1-11-5-13(20)9-14(6-11)22-16-7-12(2)8-17-15(16)10-18(23-17)19(3,4)21/h5-9,18,20-21H,10H2,1-4H3/t18-/m1/s1

> <INCHI_KEY>
NXECJMZOUKKGPN-GOSISDBHSA-N

> <FORMULA>
C19H22O4

> <MOLECULAR_WEIGHT>
314.381

> <EXACT_MASS>
314.151809188

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
34.24359532810416

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[(2R)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol

> <JCHEM_LOGP>
4.145844447666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.296674292424708

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.221726597718478

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1064362630238023

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
89.15439999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-{[(2R)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       8.788   8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.788   6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.122   6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.122   4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.455   3.850   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.788   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.454   4.620   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.121   3.850   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.788  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.877   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.663   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.877   2.310   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.877  -0.770   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       3.322  -0.476   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.454   6.160   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   23                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14    9   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   17   14                                                       
CONECT   23    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
a,a,6-Trimethyl-4-(3-hydroxy-5-methylphenoxy)-2,3-dihydrobenzofuran-2b-methanol	Generator
Α,α,6-trimethyl-4-(3-hydroxy-5-methylphenoxy)-2,3-dihydrobenzofuran-2β-methanol	Generator

Chemical Formula

C₁₉H₂₂O₄

Average Mass

314.3810 Da

Monoisotopic Mass

314.15181 Da

IUPAC Name

3-{[(2R)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol

Traditional Name

3-{[(2R)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol

CAS Registry Number

Not Available

SMILES

CC1=CC2=C(C[C@@H](O2)C(C)(C)O)C(OC2=CC(C)=CC(O)=C2)=C1

InChI Identifier

InChI=1S/C19H22O4/c1-11-5-13(20)9-14(6-11)22-16-7-12(2)8-17-15(16)10-18(23-17)19(3,4)21/h5-9,18,20-21H,10H2,1-4H3/t18-/m1/s1

InChI Key

NXECJMZOUKKGPN-GOSISDBHSA-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 diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Diarylethers

Alternative Parents

Substituents

Diaryl ether
Coumaran
Phenoxy compound
Phenol ether
M-cresol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Tertiary alcohol
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Alcohol
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	4.15	ChemAxon
pKa (Strongest Acidic)	9.22	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	89.15 m³·mol⁻¹	ChemAxon
Polarizability	34.24 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

78440737

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122368704

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol (NP0227866)

MOL for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

3D MOL for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

3D SDF for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

3D-SDF for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

PDB for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

3D PDB for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

SMILES for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

INCHI for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

Structure for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)

3D Structure for NP0227866 (3-{[(2r)-2-(2-hydroxypropan-2-yl)-6-methyl-2,3-dihydro-1-benzofuran-4-yl]oxy}-5-methylphenol)