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5-Bromo-2-methylpyridine, 98%|255454|3430-13-5

5-Bromo-2-methylpyridine, 98%

Cat. No JK255454_5_G
J&K Chemical

Product Information

Product Name
5-Bromo-2-methylpyridine, 98%
Brand Name
J&K
Product Number
255454
CAS
3430-13-5
Molecular Formula
C6H6BrN
Molecular Weight
172.02
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
5-Bromo-2-picoline
PubChem CID
1201020
IUPAC Name
5-bromo-2-methylpyridine
InChI Key
OFKWIQJLYCKDNY-UHFFFAOYSA-N
SMILES
CC1=NC=C(C=C1)Br

Properties

Melting Point
32-36

Safety Information

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 Data Source From Pubchem

Total Syntheses of Deuterated Drugs: A Comprehensive Review
Publication Name: Topics in current chemistry (Cham)
Publication Date: 2025-08-21
DOI: 10.1007/s41061-025-00515-x

Synthesis of ( ±)-rupestine A and ( ±)-rupestine J, structural reassignment of rupestine A via ECD analysis
Publication Name: Chemical Papers
Publication Date: 2021-06-07
DOI: 10.1007/s11696-021-01721-9

Synthesis of Crizotinib and Etoricoxib
Publication Name: Synfacts
Publication Date: 2019-01-18
DOI: 10.1055/s-0037-1612025

Sulfur-Centered Radicals: Radical Transposition for the Generation of Thiyl Radicals and Coupling with Aryl Bromides
Publication Name: Science of Synthesis
Publication Date: 2019

Nano-Pd/Al(OH)3-Catalyzed Suzuki–Miyaura Coupling Reaction of Potassium Aryl- and Heteroaryltrifluoroborates with Electrophiles in Alcohols
Publication Name: Synlett
Publication Date: 2016-01-05
DOI: 10.1055/s-0035-1561302

5-Bromo-2-methylpyridine, 98%

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