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3-Bromo-4-methylpyridine

Product Name
3-Bromo-4-methylpyridine
CAS No.
3430-22-6
Chemical Name
3-Bromo-4-methylpyridine
Synonyms
4-Meth;yihebio;3-BROMO-4-PICOLINE;Bromomethylpyridine;3-Bromo-4-methylpyri;3-BROMO-4-METHYLPYRIDINE;4-METHYL-3-BROMOPYRIDINE;3-Bromo-4-methylpyridins;Pyridine, 3-broMo-4-Methyl-;3--4- MethylpyridinebroMide
CBNumber
CB6338781
Molecular Formula
C6H6BrN
Formula Weight
172.02
MOL File
3430-22-6.mol
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3-Bromo-4-methylpyridine Property

Boiling point:
199-200 °C(lit.)
Density 
1.549 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.56(lit.)
Flash point:
175 °F
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform, Methanol
pka
3.54±0.18(Predicted)
form 
Liquid
Specific Gravity
1.549
color 
Clear colorless to yellow
BRN 
878354
InChI
InChI=1S/C6H6BrN/c1-5-2-3-8-4-6(5)7/h2-4H,1H3
InChIKey
GSQZOLXWFQQJHJ-UHFFFAOYSA-N
SMILES
C1=NC=CC(C)=C1Br
CAS DataBase Reference
3430-22-6(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36-2636
RIDADR 
Cool, dry,tightly closed
WGK Germany 
3
HazardClass 
IRRITANT
PackingGroup 
III
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
548030
Product name
3-Bromo-4-methylpyridine
Purity
96%
Packaging
1g
Price
$30.1
Updated
2023/06/20
Sigma-Aldrich
Product number
548030
Product name
3-Bromo-4-methylpyridine
Purity
96%
Packaging
5g
Price
$77.7
Updated
2023/06/20
TCI Chemical
Product number
B2831
Product name
3-Bromo-4-methylpyridine
Purity
>98.0%(GC)(T)
Packaging
1g
Price
$16
Updated
2025/07/31
TCI Chemical
Product number
B2831
Product name
3-Bromo-4-methylpyridine
Purity
>98.0%(GC)(T)
Packaging
5g
Price
$33
Updated
2025/07/31
TCI Chemical
Product number
B2831
Product name
3-Bromo-4-methylpyridine
Purity
>98.0%(GC)(T)
Packaging
25g
Price
$98
Updated
2025/07/31
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3-Bromo-4-methylpyridine Chemical Properties,Usage,Production

Chemical Properties

Clear Liquid

Uses

An intermediate of pyridinyl pyrrole compounds as proton pump inhibitors with improved gastric acid secretion suppressive activity

Uses

3-Bromo-4-methylpyridine may be used as a building block in the preparation of:

  • substituted 4-(2,2-diphenylethyl)pyridine-N-oxides for use as potent phosphodiesterase type 4 (PDE4) inhibitors
  • benzodiazepine site ligands bearing tricyclic pyridone moiety for human GABAA receptor
  • a novel isomer of ascididemin
  • 3-bromopyridine-4-carbonitrile

Synthesis

108-89-4

3430-22-6

The general procedure for the synthesis of 4-methyl-3-bromopyridine from 4-methylpyridine was as follows: 0.054 mol of 4-methylpyridine was added to a 60 mL constant pressure dropping funnel. Under nitrogen protection and stirring conditions at room temperature, it was slowly added dropwise to a mixture consisting of 0.07 mol AlCl3 and 0.01 mol potassium bromide, and the reaction mixture was stirred for 1 hour. A condensing unit was installed, heated to 120°C, and 0.07 mol of bromine was added slowly dropwise for about 1 hour dropwise. Heating and stirring were continued at 120°C for 26 hours. Upon completion of the reaction, the reaction solution was cooled to room temperature and slowly poured into crushed ice with stirring. The pH was adjusted to neutral by the addition of sodium hydroxide solution and stirred until completely dissolved. The aqueous layer was extracted with dichloromethane, the organic layers were combined and the solvent was recovered by steam distillation. The resulting oily product was purified by column chromatography (eluent ratio of VP petroleum ether: ethyl acetate = 6:1) to give 5.3 g of 3-bromo-4-methylpyridine in the form of a tan oil with a purity of 99.9% and a yield of 57%.

References

[1] Patent: CN106243022, 2016, A. Location in patent: Paragraph 0067-0069
[2] Patent: WO2014/97150, 2014, A1. Location in patent: Page/Page column 22-23
[3] Patent: US2005/80085, 2005, A1. Location in patent: Page/Page column 12
[4] Patent: US5294610, 1994, A

3-Bromo-4-methylpyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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3-Bromo-4-methylpyridine Suppliers

TCI AMERICA
Tel
800-4238616
Fax
+1-888-520-1075 / +1-503-283-1987
Email
sales@tciamerica.com
Country
Americas
ProdList
23653
Advantage
75
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View Lastest Price from 3-Bromo-4-methylpyridine manufacturers

Shaanxi Dideu New Materials Co. Ltd
Product
3-Bromo-4-methylpyridine 3430-22-6
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98.0%
Supply Ability
10000KGS
Release date
2025-05-30
Hebei Chuanghai Biotechnology Co., Ltd
Product
3-Bromo-4-methylpyridine 3430-22-6
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-31
Henan Aochuang Chemical Co.,Ltd.
Product
3-Bromo-4-methylpyridine 3430-22-6
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1Ton
Release date
2022-09-27

3430-22-6, 3-Bromo-4-methylpyridineRelated Search:


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  • 3430-22-6
  • 3420-22-6
  • 7441-89-0
  • C6H6BR
  • Building Blocks
  • Halopyridines
  • Bromopyridines
  • Pyridines
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Brominated heterocyclic series
  • Pyridine Series
  • Heterocycles
  • Heterocycle-Pyridine series
  • alkyl bromide
  • Bromopyridines
  • Halopyridines
  • Aromatics Compounds
  • Halides
  • Pyridines derivates
  • Aromatics
  • C6Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • blocks
  • Bromides
  • Pyridines
  • Pyridine
  • Pyridines, Pyrimidines, Purines and Pteredines