5-(Bromomethyl)-2-methylthiazole

5-(Bromomethyl)-2-methylthiazole Suppliers list
Company Name: Cool Pharm, Ltd  
Tel: 021-60455363 18019463053
Email: sales@coolpharm.com
Company Name: Yancheng Schiemann Biological Technology Co.,Ltd  
Tel: 0515-88280676; 18921872653
Email: sales@ximanbio.com
Company Name: BePharm Ltd  
Tel: 400-685-9117
Email: market@bepharm.com
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: Aikon International Limited  
Tel: 025-58859352 19370895928
Email: sales01@aikonchem.com
5-(Bromomethyl)-2-methylthiazole Basic information
Product Name:5-(Bromomethyl)-2-methylthiazole
Synonyms:5-(BROMOMETHYL)-2-METHYL-1,3-THIAZOLE;5-(Bromomethyl)-2-methylthiazole;Thiazole, 5-(bromomethyl)-2-methyl-
CAS:838892-95-8
MF:C5H6BrNS
MW:192.08
EINECS:
Product Categories:
Mol File:838892-95-8.mol
5-(Bromomethyl)-2-methylthiazole Structure
5-(Bromomethyl)-2-methylthiazole Chemical Properties
Boiling point 231.0±15.0 °C(Predicted)
density 1.629±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka2.69±0.10(Predicted)
Safety Information
MSDS Information
5-(Bromomethyl)-2-methylthiazole Usage And Synthesis
Synthesis
(2-Methyl-1,3-thiazol-5-yl)Methanol

56012-38-5

5-(Bromomethyl)-2-methylthiazole

838892-95-8

Step 2: Synthesis of 2-methyl-5-hydroxymethylthiazole At room temperature, 2-methyl-5-hydroxymethylthiazole (12 g, 0.1 mol) was dissolved in dichloromethane (500 mL) and the resulting solution was cooled to 0-5 °C in an ice water bath. Subsequently, triphenylphosphine (52 g, 0.2 mol) and carbon tetrabromide (66 g, 0.2 mol) were added to the cooled mixture in batches. After the addition was completed, the reaction mixture was allowed to warm up naturally to room temperature and stirred continuously at this temperature for 2 hours. Upon completion of the reaction, the mixture was concentrated and purified by silica gel column chromatography (eluent ratio of petroleum ether:ethyl acetate = 2:1), resulting in a yellow solid product (3.3 g, overall yield in two steps: 15%).

References[1] Patent: EP3181554, 2017, A1. Location in patent: Paragraph 0092
5-(Bromomethyl)-2-methylthiazole Preparation Products And Raw materials
Raw materials(2-Methyl-1,3-thiazol-5-yl)Methanol-->Dichloromethane-->Triphenylphosphine-->Carbon tetrabromide
Tag:5-(Bromomethyl)-2-methylthiazole(838892-95-8) Related Product Information