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Molecule
ID:19025
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₇N₃O
Molecular Mass
137.13928
Exact Mass
137.05891186
Charge
0
InChI
InChI=1S/C6H7N3O/c7-9-6(10)5-3-1-2-4-8-5/h1-4H,7H2,(H,9,10)
InChIKey
BAQLNPIEFOYKNB-UHFFFAOYSA-N
Canonic Smiles
NNC(=O)c1ccccn1
Isomeric Smiles
C(=O)(c1ncccc1)NN
Calculated Properties
JChem
Acid pKa
14.042358
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-0.30502123
LogD (pH = 7.4)
-0.30441946
Log P
-0.30441168
Molar Refractivity
37.0916
Polarizability
13.714657
Polar Surface Area
68.01
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Registration numbers
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Properties
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Related Proteins
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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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Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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PubChem SID
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PubChem CID
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MDL Number
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CAS Number
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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TRC
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
255881
Commercial Catalog
Matrix Scientific
021267
TRC
I821455
Enamine
EN300-03839
Bide Pharmatech
BD78283
Names and Identifiers
IUPAC name
pyridine-2-carbohydrazide
Synonyms
Pyridine-2-carboxylic acid hydrazide
Picolinoyl Hydrazide
2-Pyridinecarboxylic Hydrazide
Pyridine-2-carbohydrazide
2-Isoniazid
Picolinoylhydrazine
Picolinic Hydrazide
2-Pyridinecarboxylic Acid Hydrazide, Picolinic Acid, 2-(Hydrazinocarbonyl)pyridine
Picolinohydrazide
IUPAC Traditional name
pyridine-2-carbohydrazide
Registration numbers
PubChem SID
160982332
PubChem CID
255881
MDL Number
MFCD00059782
CAS Number
1452-63-7
Molecule Details
TRC
I821455
An impurity of Isoniazid (I821450), which is an antibiotic for treatment of Mycobacterium tuberculosis and inhibits mycolic acid biosynthesis. Intermediate used for the synthesis of analogs of antitumor agent 1-acetyl-2-picolinoylhydrazine.
References
PubChem Literature
From Data Sources
•
Brewer, G.A., et al.: Anal. Profiles. Drug. Subs., 6, 183 (1977)
•
Weber, W.W., et al.: Clin. Pharmacokinet., 4, 401 (1977)
•
Rutner, H., et al.: Cancer. Chem. Rep., 58, 803 (1974)
Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
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Product Information
Certificate of Analysis
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Source
95%
Source
95+%
Source
Physical Property
-0.318
Source
100 - 102°C
Source
Purity
Hydrophobicity(logP)
Melting Point