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4-Bromo-2,6-dimethylpyridine, 98%|149352|5093-70-9

4-Bromo-2,6-dimethylpyridine, 98%

Cat. No JK149352_5_G
J&K Chemical

Product Information

Product Name
4-Bromo-2,6-dimethylpyridine, 98%
Brand Name
J&K
Product Number
149352
CAS
5093-70-9
Molecular Formula
C7H8BrN
Molecular Weight
186.05
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
13081735
IUPAC Name
4-bromo-2,6-dimethylpyridine
InChI Key
VTRFAYHJKSKHGY-UHFFFAOYSA-N
SMILES
CC1=CC(=CC(=N1)C)Br

Properties

Melting Point
28-32
Flash Point
93.8

Safety Information

GHS Symbols
Hazard Symbol
Hazard Symbol
Signal Word
Danger
Hazard Statement
H302
H315
H318
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P354+P338
P304+P340
P403+P233

References

Increased rigidity and bioisosteric replacement in the design, synthesis and preliminary evaluation of novel, functionalized 3,3-dialkyl-γ-butyrolactones as sigma-2 ligands
Publication Name: Medicinal Chemistry Research
Publication Date: 2023-12-29
DOI: 10.1007/s00044-023-03182-z

C-H alkylation of pyridines with olefins catalyzed by imidazolin-2-iminato-ligated rare-earth alkyl complexes
Publication Name: Science China Chemistry
Publication Date: 2023-05-10
DOI: 10.1007/s11426-023-1588-8

Via Hetaryl–Metal Coordination
Publication Name: Science of Synthesis
Publication Date: 2022

Two-Component Reductive Dicarbofunctionalization of Alkenes
Publication Name: Science of Synthesis
Publication Date: 2022

Photocatalyst Energy-Transfer-Mediated C—O Bond Formation: Coupling of Carboxylic Acids with Aryl Bromides
Publication Name: Science of Synthesis
Publication Date: 2019

4-Bromo-2,6-dimethylpyridine, 98%

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