NP-MRD: Showing NP-Card for 3-(3,4-dimethoxyphenyl)propanimidic acid (NP0275569)

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Record Information

Version

2.0

Created at

2022-09-08 23:21:20 UTC

Updated at

2022-09-08 23:21:21 UTC

NP-MRD ID

NP0275569

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(3,4-dimethoxyphenyl)propanimidic acid

Description

3-(3,4-Dimethoxyphenyl)propanimidic acid belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups. 3-(3,4-dimethoxyphenyl)propanimidic acid is found in Piper sintenense. 3-(3,4-Dimethoxyphenyl)propanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 30  0  0  0  0  0  0  0  0999 V2000
   -3.9947    2.4671   -0.7275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4668    1.1813   -0.5607 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1663    0.9058   -0.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2224    1.8805    0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0686    1.5172    0.4087 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4499    0.1995    0.5357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8597   -0.1405    0.9300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6947   -0.2735   -0.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0833   -0.6080    0.0776 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0247   -0.7733   -0.9822 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864   -0.7327    1.2772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4893   -0.7789    0.2929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7831   -0.4120   -0.0700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7070   -1.4046   -0.3083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3807   -2.7674   -0.1958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2994    3.1308   -1.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1778    2.8762    0.3002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9817    2.3748   -1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5197    2.9040   -0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8226    2.2843    0.6039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8225   -1.0774    1.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3041    0.6432    1.5751 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3270   -1.1318   -0.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6476    0.6079   -0.9501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8730   -1.4835   -1.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8698   -0.1849   -1.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1932   -1.8165    0.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9185   -2.9436    0.8186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2944   -3.3892   -0.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6388   -3.0548   -0.9652 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  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
  6 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 13  3  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  4 19  1  0
  5 20  1  0
  7 21  1  0
  7 22  1  0
  8 23  1  0
  8 24  1  0
 10 25  1  0
 10 26  1  0
 12 27  1  0
 15 28  1  0
 15 29  1  0
 15 30  1  0
M  END


  Mrv1533004251516132D          

 15 15  0  0  0  0            999 V2000
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   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
    0.7145   -0.4125    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   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   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
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0275569

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(CCC(N)=O)C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C11H15NO3/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3,5,7H,4,6H2,1-2H3,(H2,12,13)

> <INCHI_KEY>
CMEASCHYTXEXMS-UHFFFAOYSA-N

> <FORMULA>
C11H15NO3

> <MOLECULAR_WEIGHT>
209.245

> <EXACT_MASS>
209.105193347

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
22.337631073404253

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(3,4-dimethoxyphenyl)propanamide

> <ALOGPS_LOGP>
1.10

> <JCHEM_LOGP>
0.9332776253333335

> <ALOGPS_LOGS>
-2.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.957916334039627

> <JCHEM_PKA_STRONGEST_BASIC>
-1.7105836770930627

> <JCHEM_POLAR_SURFACE_AREA>
61.55

> <JCHEM_REFRACTIVITY>
56.71520000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.77e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(3,4-dimethoxyphenyl)propanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       1.334  -5.390   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    6   13                                                       
CONECT   13   12    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

View in JSmol

Synonyms

Value	Source
3-(3,4-Dimethoxyphenyl)propanimidate	Generator

Chemical Formula

C₁₁H₁₅NO₃

Average Mass

209.2450 Da

Monoisotopic Mass

209.10519 Da

IUPAC Name

3-(3,4-dimethoxyphenyl)propanamide

Traditional Name

3-(3,4-dimethoxyphenyl)propanamide

CAS Registry Number

Not Available

SMILES

COC1=CC=C(CCC(N)=O)C=C1OC

InChI Identifier

InChI=1S/C11H15NO3/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3,5,7H,4,6H2,1-2H3,(H2,12,13)

InChI Key

CMEASCHYTXEXMS-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
Piper sintenense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Methoxybenzenes

Direct Parent

Dimethoxybenzenes

Alternative Parents

Substituents

O-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Anisole
Phenol ether
Alkyl aryl ether
Fatty amide
Fatty acyl
Carboxamide group
Primary carboxylic acid amide
Carboxylic acid derivative
Ether
Organonitrogen compound
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Organopnictogen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
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	1.1	ALOGPS
logP	0.93	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	15.96	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	61.55 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	56.72 m³·mol⁻¹	ChemAxon
Polarizability	22.34 Å³	ChemAxon
Number of Rings	1	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

883356

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(3,4-dimethoxyphenyl)propanimidic acid (NP0275569)

MOL for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

3D MOL for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

3D SDF for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

3D-SDF for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

PDB for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

3D PDB for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

SMILES for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

INCHI for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

Structure for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)

3D Structure for NP0275569 (3-(3,4-dimethoxyphenyl)propanimidic acid)