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3-Amino-2,6-dibromopyridine, 98%|213419|39856-57-0

3-Amino-2,6-dibromopyridine, 98%

Cat. No JK213419_1_G
J&K Chemical

Product Information

Product Name
3-Amino-2,6-dibromopyridine, 98%
Brand Name
J&K
Product Number
213419
CAS
39856-57-0
Molecular Formula
C5H4Br2N2
Molecular Weight
251.91
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
817678
IUPAC Name
2,6-dibromopyridin-3-amine
InChI Key
CRTOIQFRVBJJRI-UHFFFAOYSA-N
SMILES
C1=CC(=NC(=C1N)Br)Br

Properties

Melting Point
145-149

Safety Information

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

References

Base-Mediated Cyclization
Publication Name: Science of Synthesis
Publication Date: 2016

Reactions of Pyridines, Benzopyridines, and Azapyridines with Organomagnesiums and Organolithiums
Publication Name: Metalation of Azines and Diazines
Publication Date: 2013
DOI: 10.1007/7081_2012_96

Palladium-Catalyzed One-Pot Synthesis of Pyrrole-Annulated Coumarin, Quinolone, and 7-Aza-indole Derivatives
Publication Name: Synlett
Publication Date: 2011-09-13
DOI: 10.1055/s-0030-1260312

Palladium-Mediated Reductive Heck Cyclization for the Formation of Dibenzoazepinone Framework
Publication Name: Synlett
Publication Date: 2009-10-15
DOI: 10.1055/s-0029-1218298

Transition-Metal-Catalyzed Site-Selective Cross-Coupling of Di- and Polyhalogenated Compounds
Publication Name: Synthesis
Publication Date: 2009-04-14
DOI: 10.1055/s-0029-1216632

3-Amino-2,6-dibromopyridine, 98%

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