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Molecule
ID:104927
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₀O₄
Molecular Mass
182.1733
Exact Mass
182.0579088
Charge
0
InChI
InChI=1S/C9H10O4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3,(H,10,11)
InChIKey
DAUAQNGYDSHRET-UHFFFAOYSA-N
Canonic Smiles
COc1cc(ccc1OC)C(=O)O
Isomeric Smiles
COc1c(OC)cc(cc1)C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-1.76
LogD (pH = 5.5)
-0.06
Log P
1.32
Rotatable Bonds
3
H Donor
1
H Acceptors
4
Lipinski's Rule of Five
true
Acid pKa
4.14
Polar Surface Area
55.76
Polarizability
17.89
Molar Refractivity
46.24
LOG S
-1.57
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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JChem
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Academic Data
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IUPAC Traditional name
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IUPAC name
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Molecule Details
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MP Biomedicals
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ChEBI
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
05214035
02157771
Sigma Aldrich
D131806
D3773
94872
TRC
V127560
Bide Pharmatech
BD6724
Alfa Aesar
A10167
BioBioPha
BBP01344
Academic Data
PubChem
7121
ChEBI
CHEBI:296881
Names and Identifiers
Synonyms
3,4-DIMETHOXYBENZOIC ACID
Veratric acid
藜芦酸
3,4-二甲氧基苯甲酸
3,4-二甲氧基苯甲酸
3,4-Dimethoxybenzoic acid
Veratric acid
藜芦酸
3,4-Dimethoxybenzoic acid
NSC 7721
Veratric Acid
Dimethylprotocatechuic acid
3,4-Dimethylprotocatechuic acid
Veratrylic acid
Veratric acid
3,4-Dimethoxybenzoic acid
3,4-dimethoxybenzoic acid
Dimethylprotocatechuic acid
Veratrumenoic acid
IUPAC Traditional name
veratric acid
IUPAC name
3,4-dimethoxybenzoic acid
Molecule Details
MP Biomedicals
05214035
MP Biomedicals Rare Chemical collection
Sigma Aldrich
D131806
Packaging
100 g in poly bottle
TRC
V127560
Veratric Acid is a derivative of Protocatechuic Acid. Veratric Acid is a reagent used in the production of antimicrobial agents, antifeedants, and a variety of other biologically active compounds.
ChEBI
CHEBI:296881
A member of the class of benzoic acids that is benzoic acid substituted by methoxy groups at positions 2 and 3.
References
PubChem Literature
From Data Sources
•
Alissandrakis, E., et al.: Eur. Food Res. Technol., 229, 365 (2009)
•
Pereira, L., et al.: J. Biotechnol., 139, 68 (2009)
•
Spaccini, R., et al.: Soil Biol. Biochem., 41, 1164 (2009)
•
Narasimhan, B., et al.: Eur. J. Med. Chem., 44, 689 (2009)
Bioactivity
PubChem BioAssay
Properties
•
Product Information
•
Safety Information
•
Physical Property
Properties
Product Information
Certificate of Analysis
Download link
Source
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Source
Purity
≥99%
Source
≥99.0% (HPLC)
Source
98%
Source
99+%
Source
(CH3O)2C6H3CO2H
Source
purum
Source
Safety Information
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Physical Property
179°C
Source
179-182 °C(lit.)
Source
180-182 °C
Source
172-176°C
Source
179-183°C
Source
Off-White Solid
Source
Powder
Source
Source
Download link
Source
RTECS
DG8598750
Source
GHS Signal Word
Warning
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Safety Statements
26
-
36
Source
26
-
37
Source
German water hazard class
3
Source
European Hazard Symbols
Irritant (Xi)
Source
Risk Statements
36/37/38
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Storage Condition
Refrigerator
Source
TSCA Listed
是
Source
Solubility
Methanol
Source
Chloroform
Source
Linear Formula
Grade
MSDS Link
Melting Point
Apperance
Related Proteins
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4EGN
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PDB Bank
Registration numbers
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EC Number
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PubChem CID
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PubChem SID
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MDL Number
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Beilstein Number
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Merck Index
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Reaxys Registry
•
BKMS React Database
•
BRENDA Database
•
CHEMBL
•
PubMed Citation Links
•
CHEBI ID
•
BindingDB Database
•
IEDB Database
•
HMDB Database
•
Protein Data Bank
•
BRENDA Ligand Database
•
MetaboLights Database
•
Gmelin ID
•
NMRShiftDB Database
•
ACToR Database
•
LINCS Database
•
SABIO-RK Database
•
CompTox Database
•
SureChEMBL Database
Registration numbers
CAS Number
93-07-2
EC Number
202-215-7
PubChem CID
7121
PubChem SID
162092199
24890070
24893253
85489304
MDL Number
MFCD00002500
Beilstein Number
518285
Merck Index
149953
Reaxys Registry
518285
BKMS React Database
9566
170374
7199
2494
3072
94175
9612
93934
BRENDA Database
1.1.3.7
2.1.1.25
3.1.1.20
1.10.3.2
1.2.1.3
2.4.1.65
1.2.1.67
1.14.13.82
1.14.99.15
2.1.1.67
4.2.1.1
1.2.3.1
1.11.2.1
1.2.3.9
3.5.5.1
CHEMBL
CHEMBL118903
PubMed Citation Links
3377143
25034806
22426778
8911701
23753470
23666007
CHEBI ID
CHEBI:296881
BindingDB Database
50336487
IEDB Database
119695
HMDB Database
HMDB0059763
Protein Data Bank
4egn
BRENDA Ligand Database
9612
7199
3072
9566
170374
2494
93934
94175
MetaboLights Database
MTBLS204
MTBLS1622
Gmelin ID
1007934
NMRShiftDB Database
20036240
ACToR Database
93-07-2
LINCS Database
LSM-19990
SABIO-RK Database
6888
CompTox Database
DTXSID6059077
SureChEMBL Database
SCHEMBL114848
1.2.1.29
2.4.1.136