NP-MRD: Showing NP-Card for 2-methylbutanoic acid; p-propenylanisole (NP0252357)

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Record Information

Version

2.0

Created at

2022-09-07 15:50:13 UTC

Updated at

2022-09-07 15:50:13 UTC

NP-MRD ID

NP0252357

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-methylbutanoic acid; p-propenylanisole

Description

1-Methoxy-4-(prop-1-en-1-yl)benzene; 2-methylbutanoic acid belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. 2-methylbutanoic acid; p-propenylanisole is found in Pimpinella corymbosa. Based on a literature review very few articles have been published on 1-methoxy-4-(prop-1-en-1-yl)benzene; 2-methylbutanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 39  0  0  0  0  0  0  0  0999 V2000
    4.3399   -0.0907   -0.8106 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8552   -0.1033   -0.7721 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1759    0.1317    0.3136 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7335    0.1254    0.3779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0657   -0.1306   -0.7064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4514   -0.1285   -0.6087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0758    0.1313    0.5833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4361    0.1546    0.7735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4018   -0.0820   -0.2139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2801    0.3933    1.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0844    0.3861    1.5756 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9879   -0.4628    0.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5791   -0.8126   -0.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4042    0.2940    0.2462 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0724    1.5671   -0.4541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7393   -0.1696   -0.1743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3597    0.4866   -1.0375 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2876   -1.3022    0.3749 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7654   -1.1170   -0.7133 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7449    0.4530   -1.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6960    0.4507    0.1095 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3754   -0.3260   -1.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7554    0.3456    1.2253 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3461   -0.3404   -1.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0846   -0.3303   -1.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2817    0.6354   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3929   -1.1262   -0.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3956    0.0920    0.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7055    0.6026    2.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6990    0.5905    2.4429 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0172    0.1600    1.2313 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5402    0.0171   -0.5250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5054   -1.4446    0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4969   -0.9870   -1.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2047   -1.7394    0.4141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4555    0.5048    1.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0541    1.4575   -1.5451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9333    2.2695   -0.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8556    2.0458   -0.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9891   -1.8842   -0.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 18  1  0
 16 17  2  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  4 11  1  0
 11 10  2  0
 10  7  1  0
 12 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  1
 15 37  1  0
 15 38  1  0
 15 39  1  0
 18 40  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
  6 25  1  0
  5 24  1  0
  3 23  1  0
  2 22  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
 11 30  1  0
 10 29  1  0
M  END


  Mrv1652309072217502D          

 18 17  0  0  0  0            999 V2000
   -0.6495    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6495    1.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650    1.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650    0.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7794    0.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7794   -0.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650   -1.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0650   -1.9125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7794   -2.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6495   -0.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6495    0.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9026    1.5310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4901    0.8165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9026    0.1021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7276    0.1021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4901   -0.6124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9026   -1.3269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6651   -0.6124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
  4 11  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252357

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(O)=O.COC1=CC=C(C=CC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C10H12O.C5H10O2/c1-3-4-9-5-7-10(11-2)8-6-9;1-3-4(2)5(6)7/h3-8H,1-2H3;4H,3H2,1-2H3,(H,6,7)

> <INCHI_KEY>
XZOGRWVQFHTKRV-UHFFFAOYSA-N

> <FORMULA>
C15H22O3

> <MOLECULAR_WEIGHT>
250.338

> <EXACT_MASS>
250.156894568

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
17.45933242377903

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-methoxy-4-(prop-1-en-1-yl)benzene; 2-methylbutanoic acid

> <JCHEM_LOGP>
2.9389116129999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.822404266999745

> <JCHEM_POLAR_SURFACE_AREA>
9.23

> <JCHEM_REFRACTIVITY>
47.881

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
p-propenylanisole (+-)-2-methylbutyrate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.212   4.900   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.212   3.360   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.121   2.590   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.121   1.050   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.455   0.280   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.455  -1.260   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.121  -2.030   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.121  -3.570   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.455  -4.340   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.212  -1.260   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.212   0.280   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.285   2.858   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.515   1.524   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.285   0.191   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.825   0.191   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.515  -1.143   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.285  -2.477   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       4.975  -1.143   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10    4                                                       
CONECT   12   13                                                            
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   34    0
END

View in JSmol

Synonyms

Value	Source
1-Methoxy-4-(prop-1-en-1-yl)benzene; 2-methylbutanoate	Generator

Chemical Formula

C₁₅H₂₂O₃

Average Mass

250.3380 Da

Monoisotopic Mass

250.15689 Da

IUPAC Name

1-methoxy-4-(prop-1-en-1-yl)benzene; 2-methylbutanoic acid

Traditional Name

p-propenylanisole (+-)-2-methylbutyrate

CAS Registry Number

Not Available

SMILES

CCC(C)C(O)=O.COC1=CC=C(C=CC)C=C1

InChI Identifier

InChI=1S/C10H12O.C5H10O2/c1-3-4-9-5-7-10(11-2)8-6-9;1-3-4(2)5(6)7/h3-8H,1-2H3;4H,3H2,1-2H3,(H,6,7)

InChI Key

XZOGRWVQFHTKRV-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

Species Name	Source	Reference
Pimpinella corymbosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Methoxybenzene
Styrene
Anisole
Methyl-branched fatty acid
Branched fatty acid
Alkyl aryl ether
Fatty acyl
Fatty acid
Monocyclic benzene moiety
Monocarboxylic acid or derivatives
Ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Not Available

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	2.94	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	9.23 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	47.88 m³·mol⁻¹	ChemAxon
Polarizability	17.46 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

163195813

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-methylbutanoic acid; p-propenylanisole (NP0252357)

MOL for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

3D MOL for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

3D SDF for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

3D-SDF for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

PDB for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

3D PDB for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

SMILES for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

INCHI for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

Structure for NP0252357 (2-methylbutanoic acid; p-propenylanisole)

3D Structure for NP0252357 (2-methylbutanoic acid; p-propenylanisole)