NP-MRD: Showing NP-Card for 5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate (NP0231604)

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Record Information

Version

2.0

Created at

2022-09-06 12:32:42 UTC

Updated at

2022-09-06 12:32:42 UTC

NP-MRD ID

NP0231604

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate

Description

5-Methyl-2-[(2R)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group. 5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate is found in Hymenopappus scabiosaeus and Mikania goyazensis. Based on a literature review very few articles have been published on 5-methyl-2-[(2R)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
   -4.1303    3.9560    0.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8146    3.2508    0.2604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6446    3.9393    0.0572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4604    3.2551    0.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4006    1.8655    0.2446 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9208    1.1858    0.2379 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0471   -0.1461   -0.3800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1837   -0.8790   -0.0768 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3788   -0.4222   -0.5029 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4276   -1.4192   -0.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0974   -2.7506   -0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8162   -0.9554   -0.3062 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8506    1.5976    1.3376 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0118    2.0727    0.0349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5671    1.2211    0.4407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7081   -0.1493    0.6526 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5144   -0.8966   -0.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0635   -0.2716   -1.1552 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7259   -2.3397   -0.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6336   -2.8394   -1.1743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3307   -2.6595    1.2608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8077    1.8939    0.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8809    3.3181   -0.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5000    4.1145    1.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0338    4.9081   -0.2815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6774    4.9955   -0.0918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4783    3.7790   -0.1090 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9033   -0.0857   -1.5061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2228   -0.8075   -0.0527 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6752    0.6007   -0.3533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3825   -0.5567   -1.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3211   -1.5108    1.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -3.5491    0.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5202   -2.7770   -1.6332 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9721   -2.8277   -0.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5080   -1.5642    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1428   -1.1498   -1.3489 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9447    0.0871   -0.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4918    2.3230    2.1088 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6434    0.9238    1.6915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7455   -2.8520   -0.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1419   -2.8897   -2.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5610   -2.2360   -1.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9932   -3.8816   -0.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5095   -3.0160    1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0681   -3.4598    1.1569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8014   -1.7605    1.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7384    1.3651    0.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10 12  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  6  7  1  6
  6 13  1  0
 13 14  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 22  1  0
 22 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 14  6  1  0
 15  5  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
 10 32  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
  9 30  1  0
  9 31  1  0
  7 28  1  0
  7 29  1  0
 13 39  1  0
 13 40  1  0
  4 27  1  0
  3 26  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 22 48  1  0
 19 41  1  0
 20 42  1  0
 20 43  1  0
 20 44  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
M  END


  Mrv1652309062214322D          

 22 23  0  0  1  0            999 V2000
   -1.7410    0.4531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2107    1.0850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4929    1.8603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9626    2.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1501    2.3490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802    2.9810    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0946    2.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8091    2.9810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5236    2.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2380    2.9810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9525    2.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2380    3.8060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1501    3.6130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6623    3.7563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1320    1.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9445    1.4305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2267    0.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6964    0.0233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0391    0.5120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3213   -0.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5694    1.1440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3983    0.9418    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  2  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  1  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
 10 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 15 22  2  0  0  0  0
  2 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0231604

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)COC[C@]1(CO1)C1=CC=C(C)C=C1OC(=O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O4/c1-12(2)9-20-10-18(11-21-18)15-7-6-14(5)8-16(15)22-17(19)13(3)4/h6-8,12-13H,9-11H2,1-5H3/t18-/m0/s1

> <INCHI_KEY>
SRHOLQWODNSAIG-SFHVURJKSA-N

> <FORMULA>
C18H26O4

> <MOLECULAR_WEIGHT>
306.402

> <EXACT_MASS>
306.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
34.66851939136467

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-methyl-2-[(2R)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate

> <JCHEM_LOGP>
4.222565549333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8966536291797937

> <JCHEM_POLAR_SURFACE_AREA>
48.06

> <JCHEM_REFRACTIVITY>
85.3786

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-methyl-2-[(2R)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate

> <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      -3.250   0.846   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.260   2.025   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.787   3.473   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.797   4.652   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.280   4.385   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.710   5.565   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.043   4.795   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.377   5.565   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.711   4.795   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.044   5.565   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.378   4.795   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.044   7.105   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.280   6.744   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.236   7.012   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.246   2.938   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.763   2.670   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.290   1.223   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.300   0.043   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.806   0.956   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.333  -0.491   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.796   2.135   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.743   1.758   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7   13   14                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    6   14                                                       
CONECT   14   13    6                                                       
CONECT   15    5   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   15    2                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
5-Methyl-2-[(2R)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoic acid	Generator

Chemical Formula

C₁₈H₂₆O₄

Average Mass

306.4020 Da

Monoisotopic Mass

306.18311 Da

IUPAC Name

5-methyl-2-[(2R)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate

Traditional Name

5-methyl-2-[(2R)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate

CAS Registry Number

Not Available

SMILES

CC(C)COC[C@]1(CO1)C1=CC=C(C)C=C1OC(=O)C(C)C

InChI Identifier

InChI=1S/C18H26O4/c1-12(2)9-20-10-18(11-21-18)15-7-6-14(5)8-16(15)22-17(19)13(3)4/h6-8,12-13H,9-11H2,1-5H3/t18-/m0/s1

InChI Key

SRHOLQWODNSAIG-SFHVURJKSA-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

Species Name	Source	Reference
Hymenopappus scabiosaeus	LOTUS Database	35616633
Mikania goyazensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenol esters

Sub Class

Not Available

Direct Parent

Phenol esters

Alternative Parents

Substituents

Phenol ester
Phenoxy compound
Toluene
Monocyclic benzene moiety
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	4.22	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48.06 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	85.38 m³·mol⁻¹	ChemAxon
Polarizability	34.67 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

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

163021639

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate (NP0231604)

MOL for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

3D MOL for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

3D SDF for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

3D-SDF for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

PDB for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

3D PDB for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

SMILES for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

INCHI for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

Structure for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)

3D Structure for NP0231604 (5-methyl-2-[(2r)-2-[(2-methylpropoxy)methyl]oxiran-2-yl]phenyl 2-methylpropanoate)