NP-MRD: Showing NP-Card for 3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate (NP0256449)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 21:16:48 UTC

Updated at

2022-09-07 21:16:48 UTC

NP-MRD ID

NP0256449

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate

Description

3-Formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group. 3-Formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
    7.1493    0.6871    0.3780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1467    1.1870   -0.4793 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8245    0.9285   -0.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8269    1.4021   -1.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4976    1.1570   -0.7421 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1963    0.4082    0.3892 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8108    0.1023    0.7456 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5349   -0.5690    1.7581 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2405    0.5580   -0.0450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5465    0.2503    0.3210 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4133    1.5102    0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7438    0.8533    0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8880    1.3180    1.3779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7122   -0.2286   -0.2291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8298   -1.1109   -0.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9355   -0.9188    0.1528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3712   -0.3267   -0.8487 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9262   -1.6934   -1.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6945   -2.2087   -2.3448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5914   -3.3831   -2.6787 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1887   -0.0683    1.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4962    0.1932    0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9994    1.0707    1.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0289   -0.4203    0.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1644    0.9541    0.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0858    1.9900   -1.8944 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6957    1.5125   -1.3592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6362   -0.3434    1.2279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3458    2.0917   -0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1491    2.0414    1.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5509    2.0556    2.1282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6665    1.7437    0.7093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3938    0.4826    1.9408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7490   -1.9590   -1.0722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2648    0.3711   -1.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9699   -2.3653   -0.3254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8515   -1.6267   -1.4952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3552   -1.5606   -2.8985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9158   -0.6593    2.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2638   -0.1852    1.5653 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 21  1  0
 21 22  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 22  3  1  0
 17 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
 21 39  1  0
 22 40  1  0
 10 28  1  1
 11 29  1  0
 11 30  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
 15 34  1  0
 17 35  1  6
 18 36  1  0
 18 37  1  0
 19 38  1  0
M  END


  Mrv1533004191520432D          

 22 23  0  0  0  0            999 V2000
    1.4289    9.6536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    9.2411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    8.4161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    8.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    7.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    6.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    7.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    8.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.9411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    5.5286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.5286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0964    4.2187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    3.4340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    3.4340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5315    2.7666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8671    2.0129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7615    4.2187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0231    4.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6362    3.9216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4208    4.1765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3264    2.7666    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 15 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 14 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256449

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C(=O)OC1CC(C)=C(C=O)C1CC=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H18O5/c1-11-9-16(14(7-8-18)15(11)10-19)22-17(20)12-3-5-13(21-2)6-4-12/h3-6,8,10,14,16H,7,9H2,1-2H3

> <INCHI_KEY>
OWWOTKKDRBJPNA-UHFFFAOYSA-N

> <FORMULA>
C17H18O5

> <MOLECULAR_WEIGHT>
302.326

> <EXACT_MASS>
302.11542368

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
31.60238808098572

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate

> <ALOGPS_LOGP>
2.25

> <JCHEM_LOGP>
1.6623140883333334

> <ALOGPS_LOGS>
-3.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.911321183141304

> <JCHEM_PKA_STRONGEST_BASIC>
-4.477901487422878

> <JCHEM_POLAR_SURFACE_AREA>
69.67

> <JCHEM_REFRACTIVITY>
81.2447

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.76e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       2.667  18.020   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.001  17.250   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.001  15.710   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  14.940   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335  13.400   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  12.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  13.400   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  14.940   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  11.090   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.335  10.320   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       2.667  10.320   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.667   8.780   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.913   7.875   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.437   6.410   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.897   6.410   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.992   5.164   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.619   3.757   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.421   7.875   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.043   8.351   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.188   7.320   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.652   7.796   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.343   5.164   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   12   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   14                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
3-Formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoic acid	Generator
4-Methoxybenzoate 2-(2-oxoethyl)-3-formyl-4-methyl-3-cyclopentene-1-yl ester	Generator

Chemical Formula

C₁₇H₁₈O₅

Average Mass

302.3260 Da

Monoisotopic Mass

302.11542 Da

IUPAC Name

3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate

Traditional Name

3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C(=O)OC1CC(C)=C(C=O)C1CC=O

InChI Identifier

InChI=1S/C17H18O5/c1-11-9-16(14(7-8-18)15(11)10-19)22-17(20)12-3-5-13(21-2)6-4-12/h3-6,8,10,14,16H,7,9H2,1-2H3

InChI Key

OWWOTKKDRBJPNA-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 p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

P-methoxybenzoic acids and derivatives

Alternative Parents

Substituents

P-methoxybenzoic acid or derivatives
Aromatic monoterpenoid
Benzoate ester
11-noriridane monoterpenoid
Monocyclic monoterpenoid
Monoterpenoid
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
Benzoyl
Alkyl aryl ether
Alpha-hydrogen aldehyde
Carboxylic acid ester
Carboxylic acid derivative
Ether
Carbonyl group
Organic oxygen compound
Aldehyde
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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	2.25	ALOGPS
logP	1.66	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	14.91	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	69.67 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	81.24 m³·mol⁻¹	ChemAxon
Polarizability	31.6 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

9796415

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate (NP0256449)

MOL for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

3D MOL for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

3D SDF for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

3D-SDF for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

PDB for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

3D PDB for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

SMILES for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

INCHI for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

Structure for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)

3D Structure for NP0256449 (3-formyl-4-methyl-2-(2-oxoethyl)cyclopent-3-en-1-yl 4-methoxybenzoate)