NP-MRD: Showing NP-Card for 1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate (NP0313898)

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Record Information

Version

2.0

Created at

2022-09-11 11:42:58 UTC

Updated at

2022-09-11 11:42:58 UTC

NP-MRD ID

NP0313898

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate

Description

1-(7-Methoxy-2,2-dimethyl-2H-chromen-6-yl)ethyl 3-methylbutanoate belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. 1-(7-Methoxy-2,2-dimethyl-2H-chromen-6-yl)ethyl 3-methylbutanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 50  0  0  0  0  0  0  0  0999 V2000
    0.1102    0.4645    3.2958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1757   -0.2865    2.1490 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6402   -0.3182    1.0414 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8151    0.4306    1.0272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6557    0.4149   -0.0665 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3098   -0.3542   -1.1422 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1340   -1.0984   -1.1254 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2918   -1.0946   -0.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0024   -1.8351    0.0312 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8632   -3.1601   -0.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0374   -1.1234   -0.6187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1565   -0.7265   -0.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3024   -0.9544    1.2531 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2572   -0.0419   -0.6985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3233    0.4537    0.2309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8277    1.4858    1.1998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4708    1.0055   -0.5654 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2641   -0.4643   -2.2462 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4431    0.1240   -2.2325 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8491    0.9217   -1.0542 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8518    0.0051   -0.2838 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5596    2.1500   -1.5134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8187    1.1426   -0.1285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5183    0.1585    4.1545 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1810    0.3539    3.6388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0950    1.5277    3.1344 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0979    1.0334    1.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8528   -1.7020   -1.9745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3128   -2.0602    1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4055   -3.9676   -0.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0956   -3.0478   -1.8183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2116   -3.4294   -0.6709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7977   -0.7273   -1.4237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8507    0.7584   -1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6921   -0.4093    0.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4264    1.0515    2.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1135    2.1940    0.7473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7000    2.1131    1.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0957    1.7043    0.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1145    1.6074   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0876    0.1552   -0.8759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9596   -1.0558   -3.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1453    0.0552   -3.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8882    0.2302   -0.5333 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6088   -1.0609   -0.5447 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7116    0.1081    0.8067 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9338    2.7512   -2.1743 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4207    1.7656   -2.1457 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9676    2.7516   -0.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 20 23  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
  8  3  1  0
 23  5  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
 18 42  1  0
 19 43  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
 22 47  1  0
 22 48  1  0
 22 49  1  0
  7 28  1  0
  9 29  1  1
 10 30  1  0
 10 31  1  0
 10 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
M  END


  Mrv0541 04121516582D          

 23 24  0  0  0  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  5 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  3 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0313898

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=CC(C)(C)O2)C=C1C(C)OC(=O)CC(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O4/c1-12(2)9-18(20)22-13(3)15-10-14-7-8-19(4,5)23-16(14)11-17(15)21-6/h7-8,10-13H,9H2,1-6H3

> <INCHI_KEY>
MORVZXUBAOHUJH-UHFFFAOYSA-N

> <FORMULA>
C19H26O4

> <MOLECULAR_WEIGHT>
318.413

> <EXACT_MASS>
318.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
36.3247919380397

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(7-methoxy-2,2-dimethyl-2H-chromen-6-yl)ethyl 3-methylbutanoate

> <ALOGPS_LOGP>
4.69

> <JCHEM_LOGP>
4.238672228333333

> <ALOGPS_LOGS>
-4.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.580656404115961

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
91.07729999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.02e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.517   1.273   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.527   2.987   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   14                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    5   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13    3   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
1-(7-Methoxy-2,2-dimethyl-2H-chromen-6-yl)ethyl 3-methylbutanoic acid	Generator

Chemical Formula

C₁₉H₂₆O₄

Average Mass

318.4130 Da

Monoisotopic Mass

318.18311 Da

IUPAC Name

1-(7-methoxy-2,2-dimethyl-2H-chromen-6-yl)ethyl 3-methylbutanoate

Traditional Name

1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=CC(C)(C)O2)C=C1C(C)OC(=O)CC(C)C

InChI Identifier

InChI=1S/C19H26O4/c1-12(2)9-18(20)22-13(3)15-10-14-7-8-19(4,5)23-16(14)11-17(15)21-6/h7-8,10-13H,9H2,1-6H3

InChI Key

MORVZXUBAOHUJH-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 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
Anisole
Alkyl aryl ether
Fatty acid ester
Fatty acyl
Benzenoid
Carboxylic acid ester
Carboxylic acid derivative
Ether
Oxacycle
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
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	4.69	ALOGPS
logP	4.24	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	91.08 m³·mol⁻¹	ChemAxon
Polarizability	36.32 Å³	ChemAxon
Number of Rings	2	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

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DrugBank ID

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Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

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PDB ID

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ChEBI ID

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Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate (NP0313898)

MOL for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

3D MOL for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

3D SDF for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

3D-SDF for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

PDB for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

3D PDB for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

SMILES for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

INCHI for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

Structure for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)

3D Structure for NP0313898 (1-(7-methoxy-2,2-dimethylchromen-6-yl)ethyl 3-methylbutanoate)