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Molecule
ID:58575
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₈O₄
Molecular Mass
168.14672
Exact Mass
168.04225874
Charge
0
InChI
InChI=1S/C8H8O4/c1-12-7-3-2-5(8(10)11)4-6(7)9/h2-4,9H,1H3,(H,10,11)
InChIKey
LBKFGYZQBSGRHY-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cc1O)C(=O)O
Isomeric Smiles
c1(c(ccc(c1)C(=O)O)OC)O
Calculated Properties
JChem
LogD (pH = 7.4)
-1.90
LogD (pH = 5.5)
-0.20
Log P
1.17
Rotatable Bonds
2
H Donor
2
H Acceptors
4
Lipinski's Rule of Five
true
Acid pKa
4.15
Polar Surface Area
66.76
Polarizability
15.89
Molar Refractivity
41.76
LOG S
-1.13
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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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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Quote
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General Information
Calculated Properties
•
RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
Properties
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Safety Information
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
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ChEBI
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR17911
MP Biomedicals
02155134
InterBioScreen
BB_NC-2259
STOCK1N-76973
Matrix Scientific
063756
Sigma Aldrich
220108
Enamine
EN300-99197
Bide Pharmatech
BD11151
Alfa Aesar
A13709
Academic Data
PubChem
12575
ChEBI
CHEBI:63798
Names and Identifiers
IUPAC Traditional name
isovanillic acid
IUPAC name
3-hydroxy-4-methoxybenzoic acid
Synonyms
3-Hydroxy-4-methoxybenzoic acid
3-Hydroxy-4-methoxybenzoic acid
ISOVANILLIC ACID
异香草酸
Isovanillic acid
3-羟基-4-甲氧基苯甲酸
Isovanillic acid
2-Methoxy-5-carboxyphenol
5-Carboxyguaiacol
4-Carboxy-2-hydroxyanisole
3-Hydroxy-p-anisic acid
3-Hydroxy-4-methoxybenzoic acid
3-羟基-4-甲氧基苯甲酸
3-hydroxy-p-anisic acid
Acide isovanillique
Isovanillic acid
3-hydroxy-4-methoxybenzoic acid
3-Hydroxyanisic acid
Registration numbers
EC Number
211-430-5
CAS Number
645-08-9
MDL Number
MFCD00002507
PubChem SID
24853164
162063338
135611036
Beilstein Number
2208365
PubChem CID
12575
Reaxys Registry
2208365
MetaboLights Database
MTBLS2330
MTBLS392
MTBLS4820
MTBLS1906
BRENDA Ligand Database
50510
105012
32068
18302
BRENDA Database
2.1.1.6
1.2.1.3
1.2.1.7
1.17.3.2
1.14.13.24
1.14.13.82
2.1.1.291
2.1.1.67
1.2.1.67
1.2.1.28
CompTox Database
DTXSID40214745
BindingDB Database
50405313
HMDB Database
HMDB0060003
SABIO-RK Database
12714
14171
CHEBI ID
CHEBI:63798
SureChEMBL Database
SCHEMBL180473
NMRShiftDB Database
20039584
PubMed Citation Links
24820992
24956816
23477143
CHEMBL
CHEMBL88700
BKMS React Database
105012
18302
50510
32068
ACToR Database
645-08-9
UniProt Database
Q6WUC2
Molecule Details
MP Biomedicals
02155134
(3-Hydroxy-4-methoxybenzoic acid) Crystalline
Sigma Aldrich
220108
Packaging
25 g in poly bottle
5 g in glass bottle
ChEBI
CHEBI:63798
A methoxybenzoic acid that is 4-methoxybenzoic acid bearing a hydroxy substituent at position 3.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
MDL Number
•
PubChem SID
•
Beilstein Number
•
PubChem CID
•
Reaxys Registry
•
MetaboLights Database
•
BRENDA Ligand Database
•
BRENDA Database
•
CompTox Database
•
BindingDB Database
•
HMDB Database
•
SABIO-RK Database
•
CHEBI ID
•
SureChEMBL Database
•
NMRShiftDB Database
•
PubMed Citation Links
•
CHEMBL
•
BKMS React Database
•
ACToR Database
•
UniProt Database
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
BZ4850000
Source
Room Temperature (15-30°C)
Source
Warning
Source
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
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
H315
-
H319
-
H335
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
Irritant (Xi)
36/37/38
Source
26
-
36
Source
26
-
37
Source
3
Source
Physical Property
250-253°C
Source
250-253 °C(lit.)
Source
250 - 253°C
Source
251-255°C
Source
1.355
Source
Product Information
Download link
Source
HOC6H3(OCH3)CO2H
Source
97%
Source
95%
Source
97+%
Source
Genuine Natural Compounds
Source
Source
Source
RTECS
Storage Condition
GHS Signal Word
GHS Precautionary statements
GHS Pictograms
GHS Hazard statements
Personal Protective Equipment
European Hazard Symbols
Risk Statements
Safety Statements
German water hazard class
Melting Point
Hydrophobicity(logP)
Certificate of Analysis
Linear Formula
Purity
Classification