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Molecule
ID:43073
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₄N₂O₂
Molecular Mass
148.11886
Exact Mass
148.02727738
Charge
0
InChI
InChI=1S/C7H4N2O2/c8-3-5-1-2-6(7(10)11)9-4-5/h1-2,4H,(H,10,11)
InChIKey
HRLVPHGCEGTVLK-UHFFFAOYSA-N
Canonic Smiles
N#Cc1ccc(nc1)C(=O)O
Isomeric Smiles
c1(cnc(cc1)C(=O)O)C#N
Calculated Properties
JChem
Acid pKa
3.2209482
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
-1.6124164
LogD (pH = 7.4)
-2.7884831
Log P
0.6551028
Molar Refractivity
36.5069
Polarizability
13.662436
Polar Surface Area
73.98
Rotatable Bonds
1
Lipinski's Rule of Five
true
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
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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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Academic Data
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IUPAC name
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IUPAC Traditional name
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Synonyms
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CAS Number
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MDL Number
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PubChem CID
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PubChem SID
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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TRC
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Key Organics
BB-0611
Matrix Scientific
046387
Sigma Aldrich
735361
TRC
C982085
Chemik
CHH00134
Enamine
EN300-72520
Bide Pharmatech
BD103766
Alfa Aesar
H33722
A&J Pharmtech
AJA-O21714
Academic Data
PubChem
12400734
Names and Identifiers
IUPAC name
5-cyanopyridine-2-carboxylic acid
IUPAC Traditional name
5-cyanopyridine-2-carboxylic acid
Synonyms
5-Cyano-2-pyridinecarboxylic acid
5-Cyanopicolinic acid
5-Cyanopicoliniic Acid
5-Cyanopicolinic Acid
5-Cyanopyridine-2-carboxylic acid
5-Cyano-2-pyridinecarboxylic Acid
5-cyanopyridine-2-carboxylic acid
Registration numbers
CAS Number
53234-55-2
MDL Number
MFCD09152775
PubChem CID
12400734
PubChem SID
162047836
Molecule Details
Sigma Aldrich
735361
Packaging
1 g in glass bottle
TRC
C982085
5-Cyanopicolinic Acid is a substituted picolinic acid tested for inhibition of DBM (Dopamine β-monooxygenase) from bovine adrenal medulla.
References
PubChem Literature
From Data Sources
•
Brenner, M., et al.: Biochemistry, 28, 4664 (1970)
•
Evans, J., et al.: J. Biol. Chem., 278, 49691 (1970)
•
Nagatsu, T., et al.: Biochem. Pharmacol., 19, 35 (1970)
Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Store under N2
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
45
Source
26
-
36/37/39
-
60
Source
Danger
Source
2-8°C
Source
3
Source
Toxic (T)
P301+P310
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
25
Source
20/21/22
-
36/37/38
Source
H301
Source
H331
-
H302
-
H312
-
H315
-
H319
-
H335
Source
6.1
Source
III
Source
UN3439
Source
Product Information
>95%
Source
97%
Source
95%
Source
95+%
Source
98%
Source
C7H4N2O2
Source
Download link
Source
Physical Property
212 - 214 °C
Source
210-215 °C
Source
199 - 201°C
Source
212-214°C
Source
0.508
Source
Source
Source
Harmful (X)
Source
Storage Condition
GHS Pictograms
Safety Statements
GHS Signal Word
Storage Temperature
German water hazard class
European Hazard Symbols
GHS Precautionary statements
Risk Statements
GHS Hazard statements
Hazard Class
Packing Group
UN Number
Purity
Empirical Formula (Hill Notation)
Certificate of Analysis
Melting Point
Hydrophobicity(logP)