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Molecule
ID:16370
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₅NO₄
Molecular Mass
167.1189
Exact Mass
167.02185765
Charge
0
InChI
InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-3-5(4)7(11)12/h1-3H,(H,9,10)(H,11,12)
InChIKey
MUYSADWCWFFZKR-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1cnccc1C(=O)O
Isomeric Smiles
c1nccc(c1C(=O)O)C(=O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-5.95
LogD (pH = 5.5)
-3.31
Log P
-0.03
Rotatable Bonds
2
H Donor
2
H Acceptors
5
Lipinski's Rule of Five
true
Acid pKa
2.83
Polar Surface Area
87.49
Polarizability
14.27
Molar Refractivity
38.41
LOG S
-0.44
Data Source
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Names and Identifiers
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Properties
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
Properties
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Physical Property
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Product Information
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
018349
Apollo Scientific
OR28966
InterBioScreen
BB_SC-3459
Sigma Aldrich
P64006
Bide Pharmatech
BD8721
Alfa Aesar
A14580
A&J Pharmtech
AJA-O1841
Academic Data
PubChem
10273
ChEBI
CHEBI:46860
Names and Identifiers
IUPAC name
pyridine-3,4-dicarboxylic acid
Synonyms
Pyridine-3,4-dicarboxylic acid
Cinchomeronic acid
3,4-Dicarboxypyridine
3,4-吡啶二羧酸
辛可部酸
3,4-Pyridinedicarboxylic acid
Pyridine-3,4-dicarboxylic acid
吡啶-3,4-二羧酸
3,4-Pyridinedicarboxylic acid
3,4-pyridinedicarboxylic acid
cinchomeronic acid
Cinchomeronic acid
IUPAC Traditional name
3,4-pyridinedicarboxylic acid
cinchomeronic acid
Molecule Details
Sigma Aldrich
P64006
Packaging
25 g in poly bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
ca 262°C(dec)
Source
262(dec.)°C
Source
262 °C (dec.)(lit.)
Source
ca 255°C dec.
Source
Product Information
Purity
98%
Source
97%
Source
C7H5NO4
Source
Safety Information
IRRITANT
Source
Irritant/Store under Argon
Source
Download link
Source
Download link
Source
false
Source
否
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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
Safety Statements
26
-
36
Source
26
-
37
Source
European Hazard Symbols
Irritant (Xi)
Source
German water hazard class
3
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Risk Statements
36/37/38
Source
Empirical Formula (Hill Notation)
Storage Warning
MSDS Link
TSCA Listed
Registration numbers
CAS Number
490-11-9
MDL Number
MFCD00006392
Beilstein Number
137242
EC Number
207-705-4
Merck Index
142283
PubChem SID
160979677
24898762
26744323
PubChem CID
10273
BRENDA Ligand Database
36292
BRENDA Database
3.5.2.6
1.14.20.6
6.3.5.4
BindingDB Database
26117
CHEMBL
CHEMBL261326
CompTox Database
DTXSID70197653
NMRShiftDB Database
20032290
ACToR Database
514-05-6
490-11-9
BKMS React Database
36292
Gmelin ID
487254
SureChEMBL Database
SCHEMBL71335
CHEBI ID
CHEBI:46860
Related Proteins
No Data Available
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Related Proteins
Registration numbers
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CAS Number
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MDL Number
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Beilstein Number
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EC Number
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Merck Index
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PubChem SID
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PubChem CID
•
BRENDA Ligand Database
•
BRENDA Database
•
BindingDB Database
•
CHEMBL
•
CompTox Database
•
NMRShiftDB Database
•
ACToR Database
•
BKMS React Database
•
Gmelin ID
•
SureChEMBL Database
•
CHEBI ID