NP-MRD: Showing NP-Card for 2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid (NP0293301)

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Record Information

Version

2.0

Created at

2022-09-10 01:14:48 UTC

Updated at

2022-09-10 01:14:48 UTC

NP-MRD ID

NP0293301

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid

Description

SCHEMBL8429017 belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. 2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid is found in Senna auriculata. Based on a literature review very few articles have been published on SCHEMBL8429017.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 48  0  0  0  0  0  0  0  0999 V2000
   -6.2298    0.8354    1.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3660    0.8799   -0.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9311    0.5354    0.2557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8565   -0.8420    0.8654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3270   -1.8512   -0.1262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1074    0.6394   -0.9820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6835    0.3103   -0.7117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0421    1.2191    0.2945 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3948    0.8703    0.5539 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2198    0.9608   -0.6717 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683    0.6836   -0.5472 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1121   -0.4868   -0.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2139   -1.3743    0.1249 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4838   -0.8686    0.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7344   -2.1748    0.4567 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9832   -2.6849    0.6586 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0487   -1.8606    0.4136 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8518   -0.5798   -0.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5532   -0.0573   -0.2234 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4215    1.3010   -0.6771 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3829    1.8975   -0.9024 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6141    2.0460   -0.8925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0388    1.5894    0.9644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6018    1.1850    1.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6455   -0.1534    1.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3190    1.9497   -0.4753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7174    0.2930   -0.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5821    1.3160    0.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8108   -1.0239    1.1700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4553   -0.8857    1.8041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5143   -2.5962   -0.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2243   -2.3695    0.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6412   -1.4269   -1.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5254    0.0919   -1.8504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1388    1.7261   -1.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1156    0.4632   -1.6821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5187   -0.7328   -0.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1838    2.2696   -0.0253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6444    1.1363    1.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4338   -0.1740    0.9450 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7509    1.5968    1.3270 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0807    1.9322   -1.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8171    0.1919   -1.4031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8953   -2.8337    0.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1659   -3.6907    0.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0612   -2.2141    0.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6923    0.0650   -0.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7411    2.8970   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
 19 14  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 18 47  1  0
 22 48  1  0
M  END


  Mrv1652309102203142D          

 22 22  0  0  0  0            999 V2000
    3.0979   -3.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8905   -3.5771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4850   -4.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4942   -5.1788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2776   -3.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8721   -4.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6647   -4.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2592   -4.8356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0518   -4.6068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6463   -5.1788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4389   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6371   -4.1492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0334   -5.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8261   -5.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4205   -5.8653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2224   -6.6661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4297   -6.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8353   -6.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0426   -6.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4482   -5.9797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8445   -7.3525    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  3  6  1  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  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 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
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0293301

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(CC)CCCCCOC(=O)C1=CC=CC=C1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O4/c1-3-14(4-2)10-6-5-9-13-22-18(21)16-12-8-7-11-15(16)17(19)20/h7-8,11-12,14H,3-6,9-10,13H2,1-2H3,(H,19,20)

> <INCHI_KEY>
SITJHLACCXDJAM-UHFFFAOYSA-N

> <FORMULA>
C18H26O4

> <MOLECULAR_WEIGHT>
306.402

> <EXACT_MASS>
306.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
34.94423511917855

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid

> <JCHEM_LOGP>
5.468067124

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0847271876269504

> <JCHEM_PKA_STRONGEST_BASIC>
-6.956425522703435

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
86.7667

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       5.783  -7.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.262  -6.677   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.372  -7.745   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.522  -9.667   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.852  -7.318   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.961  -8.386   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.441  -7.959   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.551  -9.026   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.030  -8.599   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      16.140  -9.667   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      17.619  -9.240   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      17.989  -7.745   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      18.729 -10.308   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      20.209  -9.881   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.318 -10.948   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.948 -12.443   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.469 -12.871   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.359 -11.803   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.880 -12.230   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      15.770 -11.162   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      16.510 -13.725   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₆O₄

Average Mass

306.4020 Da

Monoisotopic Mass

306.18311 Da

IUPAC Name

2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid

Traditional Name

2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid

CAS Registry Number

Not Available

SMILES

CCC(CC)CCCCCOC(=O)C1=CC=CC=C1C(O)=O

InChI Identifier

InChI=1S/C18H26O4/c1-3-14(4-2)10-6-5-9-13-22-18(21)16-12-8-7-11-15(16)17(19)20/h7-8,11-12,14H,3-6,9-10,13H2,1-2H3,(H,19,20)

InChI Key

SITJHLACCXDJAM-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
Senna auriculata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzoic acid esters

Alternative Parents

Substituents

Benzoate ester
Benzoic acid
Benzoyl
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	5.47	ChemAxon
pKa (Strongest Acidic)	3.08	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	86.77 m³·mol⁻¹	ChemAxon
Polarizability	34.94 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

67583268

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid (NP0293301)

MOL for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

3D MOL for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

3D SDF for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

3D-SDF for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

PDB for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

3D PDB for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

SMILES for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

INCHI for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

Structure for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)

3D Structure for NP0293301 (2-{[(6-ethyloctyl)oxy]carbonyl}benzoic acid)