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6-Methylpyridine-2-carboxylic acid_Molecular_structure_CAS_934-60-1)
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6-Methylpyridine-2-carboxylic acid

Catalog No. 462128 Name Sigma Aldrich
CAS Number 934-60-1 Website http://www.sigmaaldrich.com
M. F. C7H7NO2 Telephone 1-800-521-8956
M. W. 137.13598 Fax
Purity Email
Storage Chembase ID: 53615

SYNONYMS

Title
6-甲基吡啶-2-甲酸
IUPAC name
6-methylpyridine-2-carboxylic acid
IUPAC Traditional name
6-methylpyridine-2-carboxylic acid
Synonyms
NSC 26023
NSC 109143
2-Carboxy-6-methylpyridine
6-甲基-2-吡啶羧酸
6-Methylpicolinic acid

DATABASE IDS

PubChem SID 24869943
MDL Number MFCD00023481
EC Number 213-287-4
CAS Number 934-60-1

PROPERTIES

Empirical Formula (Hill Notation) C7H7NO2
Boiling Point 100 °C/4.5 mmHg(lit.)
Melting Point 120-127 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Pharmacological activity studied in regard to:
• Interactions of carrier ligands of antidiabetic metal complexes with human serum albumin1
• Ability to chelate metalloenzyme inhibitors2
• Interactions of insulin-mimetic zinc(II) complexes with cell constituents3Reactant for:
• Synthesis of inhibitors of human 11β -hydroxysteroid dehydrogenase type 14
• Lewis base organocatalysts for stereoselective hydrosilylation reactions5Biological studies of insulin-enhancing complexes6
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Pharmacological activity studied in regard to:
• Interactions of carrier ligands of antidiabetic metal complexes with human serum albumin1
• Ability to chelate metalloenzyme inhibitors2
• Interactions of insulin-mimetic zinc(II) complexes with cell constituents3Reactant for:
• Synthesis of inhibitors of human 11β -hydroxysteroid dehydrogenase type 14
• Lewis base organocatalysts for stereoselective hydrosilylation reactions5Biological studies of insulin-enhancing complexes6

REFERENCES