2-Bromo-4-fomylthiazole

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2-Bromo-4-fomylthiazole manufacturers

2-Bromo-4-fomylthiazole Basic information
Application
Product Name:2-Bromo-4-fomylthiazole
Synonyms:2-BROMO-4-CARBOXYTHIAZOLE;2-BROMO-4-FORMYLTHIAZOLE;2-BROMO-1,3-THIAZOLE-4-CARBOXALDEHYDE;2-BROMOTHIAZOLE-4-CARBALDEHYDE, 95+%;2-Bromo-4-fomylthiazole;2-Bromo-4-formylthiazole AldrichCPR;2-bromothiazole-4-carbaldehyde, 2-bromo-1,3-thiazole-4-carbaldehyde, 2-bromothiazole-4-carboxaldehyde, 2-bromo-4-formylthiazole, 2-bromo-thiazole-4-carbaldehyde, 2-bromo-4-thiazole carboxaldehyde, 2-bromo-4-thiazolecarboxaldehyde;B2070m500
CAS:5198-80-1
MF:C4H2BrNOS
MW:192.03
EINECS:218-362-5
Product Categories:Building Blocks;Thiazole;New Products for Chemical Synthesis;C3 to C7;Chemical Synthesis;Heterocyclic Building Blocks;Aldehydes;blocks;Bromides;Thiazoles
Mol File:5198-80-1.mol
2-Bromo-4-fomylthiazole Structure
2-Bromo-4-fomylthiazole Chemical Properties
Melting point 132-135
Boiling point 264.9±13.0 °C(Predicted)
density 1.920±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka-1.37±0.10(Predicted)
form Crystalline Powder
color White to yellow
InChIInChI=1S/C4H2BrNOS/c5-4-6-3(1-7)2-8-4/h1-2H
InChIKeyMNQVIZWWCRPZOK-UHFFFAOYSA-N
SMILESS1C=C(C=O)N=C1Br
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-41-43
Safety Statements 26-36/37-39
WGK Germany 3
Hazard Note Irritant/Store Cold
TSCA No
HS Code 29341000
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Skin Sens. 1
MSDS Information
2-Bromo-4-fomylthiazole Usage And Synthesis
Application2-Bromo-4-aldehydethiazole is a heterocyclic organic compound that can be used as a pharmaceutical intermediate.
Synthesis
2-BROMO-4-HYDROXYMETHYLTHIAZOLE

5198-86-7

2-Bromo-4-fomylthiazole

5198-80-1

General procedure for the synthesis of 2-bromo-4-formylthiazole from 2-bromothiazole-4-methanol: 0.22 mol of dimethylsulfoxide was dissolved in 50 mL of dichloromethane and added slowly and dropwise to 200 mL of dichloromethane solution containing 0.11 mol of oxalyl chloride over a temperature range of -75 to -65 °C. The reaction mixture was stirred at this temperature for 30 minutes. Subsequently, 0.1 mol 2-bromothiazole-4-methanol was slowly added dropwise to a 100 mL dichloromethane solution at the same temperature range. After the dropwise addition was completed, the reaction mixture continued to be stirred at -75 to -65°C for 2 hours. Next, 0.5 mol of triethylamine was slowly added dropwise while keeping the temperature constant. The temperature of the reaction mixture was gradually increased to -10 °C and maintained at this temperature for 1 hour. Upon completion of the reaction, the mixture was poured into 400 mL of aqueous solution containing 0.4 mol of sodium bicarbonate and stirred for 30 minutes. The aqueous phase was extracted with dichloromethane, the organic layers were combined and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the resulting residue was purified by column chromatography.

References[1] Russian Journal of General Chemistry, 2017, vol. 87, # 12, p. 2766 - 2775
[2] Zh. Obshch. Khim., 2017, vol. 87, # 12, p. 1947 - 1956,10
[3] Patent: WO2017/184624, 2017, A1. Location in patent: Page/Page column 185; 186
2-Bromo-4-fomylthiazole Preparation Products And Raw materials
Raw materials2-Bromo-4-hydroxymethylthiazole-->Dimethyl sulfoxide-->Dichloromethane-->Oxalyl chloride-->Triethylamine
Preparation Products2-(3-Chlorophenyl)-1,3-thiazole-4-carboxaldehyde 97
Tag:2-Bromo-4-fomylthiazole(5198-80-1) Related Product Information
Fosthiazate Methylchloroisothiazolinone/methylisothiazolinone mixture (MCIT/MIT) 2,2'-Dithiobis(benzothiazole) Thiazole-4-carboxaldehyde 2-Methyl-4-isothiazolin-3-one Benzothiazole 2-Bromo-5-methylthiazole 1-Bromododecane 2-Bromothiazole 4-Bromo-2-formylthiazole 2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester Bromine 2-Bromo-5-fomylthiazole Ethyl 2-bromothiazole-4-carboxylate 2-Bromo-4-thiazolecarboxylic acid Methyl 2-bromothiazole-4-carboxylate Ethyl 2-bromo-5-chlorothiazole-4-carboxylate Methyl 2-bromo-5-isopropyl-1,3-thiazole-4-carboxylate