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Methyl 2-aminopyridine-4-carboxylate, 98%|244284|6937-03-7

Methyl 2-aminopyridine-4-carboxylate, 98%

Cat. No JK244284_1_G
J&K Chemical

Product Information

Product Name
Methyl 2-aminopyridine-4-carboxylate, 98%
Brand Name
J&K
Product Number
244284
CAS
6937-03-7
Molecular Formula
C7H8N2O2
Molecular Weight
152.15
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
2-Aminoisonicotinic Acid Methyl Ester
PubChem CID
236984
IUPAC Name
methyl 2-aminopyridine-4-carboxylate
InChI Key
SVWWNEYBEFASMP-UHFFFAOYSA-N
SMILES
COC(=O)C1=CC(=NC=C1)N

Properties

Boiling Point
147

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H312
H315
H319
H332
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P362+P364
P332+P317
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Solvent-dependence of KI Mediated Electrosynthesis of Imidazo[1,2-a]pyridines
Publication Name: Chemical Research in Chinese Universities
Publication Date: 2023-02-18
DOI: 10.1007/s40242-023-2323-y

Fragment-based discovery of a new class of inhibitors targeting mycobacterial tRNA modification
Publication Name: Nucleic Acids Research
Publication Date: 2020-06-30
DOI: 10.1093/nar/gkaa539

New method for preparation of (2-aminopyridin-4-yl)methanol
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2015-05
DOI: 10.1134/s1070428015050280

Recent Developments in the Chemistry of Heteroaromatic N-Oxides
Publication Name: Synthesis
Publication Date: 2015-01-14
DOI: 10.1055/s-0034-1379884

An Efficient Method for the Protection of Aromatic Amines with Benzostabase and Its Utility in Anionic Aromatic Transformations
Publication Name: Synlett
Publication Date: 2013-10-07
DOI: 10.1055/s-0033-1339794

Methyl 2-aminopyridine-4-carboxylate, 98%

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