2-Bromo-4-thiazolecarboxylic acid

2-Bromo-4-thiazolecarboxylic acid Suppliers list

Company Name:	Yancheng Schiemann Biological Technology Co.,Ltd Gold
Tel:	0515-88280676; 18921872653
Email:	sales@ximanbio.com

Company Name:	3B Pharmachem (Wuhan) International Co.,Ltd.
Tel:	18930552037
Email:	3bsc@sina.com

2-Bromo-4-thiazolecarboxylic acid manufacturers

2-Bromo-4-thiazolecarboxylic acid Basic information

Product Name:	2-Bromo-4-thiazolecarboxylic acid
Synonyms:	2-BROMO-1,3-THIAZOLE-4-CARBOXYLIC ACID;2-BROMO-4-THIAZOLECARBOXYLIC ACID;2-Bromo-1,3-thiazole-4-carboxylic acid 97%;JR-14086, 2-Bromothiazole-4-carboxylic acid, 97%;4-Thiazolecarboxylic acid, 2-bromo-;2-Bromo-4-carboxy-1,3-thiazole;2-Bromothiazole-4-carboxylic Acid >;2-BROMO-1,3-THIAZOLE-4-CARBOXYLATE
CAS:	5198-88-9
MF:	C4H2BrNO2S
MW:	208.03
EINECS:
Product Categories:	ADVANCED CHEMICALS;Heterocycles;Carboxylic Acids;Thiazoles, Isothiazoles & Benzothiazoles;Organohalides;Thiazole;Carboxylic Acids;Thiazoles, Isothiazoles &Benzothiazoles;Organic acids;API intermediates;Miscellaneous;blocks;Bromides;Carboxes;Thiazoles
Mol File:	5198-88-9.mol

2-Bromo-4-thiazolecarboxylic acid Chemical Properties

Melting point	212-214
Boiling point	350.0±15.0 °C(Predicted)
density	2.062±0.06 g/cm3(Predicted)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
pka	3.13±0.10(Predicted)
form	powder to crystal
color	White to Almost white
λmax	243nm(MeOH)(lit.)
InChI	InChI=1S/C4H2BrNO2S/c5-4-6-2(1-9-4)3(7)8/h1H,(H,7,8)
InChIKey	BEGREHRAUWCAHV-UHFFFAOYSA-N
SMILES	S1C=C(C(O)=O)N=C1Br
CAS DataBase Reference	5198-88-9(CAS DataBase Reference)

Safety Information

MSDS Information

2-Bromo-4-thiazolecarboxylic acid Usage And Synthesis

Uses	Thiazole compounds are important pharmaceutical and chemical intermediates, characterized by low toxicity, excellent biological activities (such as acaricidal, bactericidal, and inhibitory effects on insect pheromone synthesis), and diverse structural variations. Thiazole 2-bromo-4-thiazolium carboxylic acid is a key intermediate in the synthesis of thiabendazole.
Chemical Properties	Pale yellow crystals
Synthesis	Ethyl 2-aminothiazole-4-carboxylate was synthesized solvent-free from thiourea and ethyl bromopyruvate as reagent, then ethyl 2-bromothiazole-4-carboxylate was obtained by high-temperature diazotization with DM SO and sodium nitrite, and finally the target 2-bromo-4-thiazolecarboxylate was obtained by saponification with potassium carbonate-methanol solution .

2-Bromo-4-thiazolecarboxylic acid Preparation Products And Raw materials

Raw materials	Methyl 2-bromothiazole-4-carboxylate-->Ethyl 2-bromothiazole-4-carboxylate
Preparation Products	2-Iodo-4-thiazolecarboxylic acid

Tag:2-Bromo-4-thiazolecarboxylic acid(5198-88-9) Related Product Information

2-Bromothiazole 2,2'-Dithiobis(benzothiazole) Benzothiazole Methylchloroisothiazolinone/methylisothiazolinone mixture (MCIT/MIT) Fosthiazate 2-Methyl-4-isothiazolin-3-one Ethyl 2-bromothiazole-4-carboxylate Ethyl 2-bromothiazole-5-carboxylate 5-Thiazolecarboxylic acid, 2,4-dibromo- Methyl 2-bromothiazole-5-carboxylate METHYL 2-BROMOTHIAZOLE-4-CARBOXYLATE ETHYL 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE 2-BROMO-5-THIAZOLECARBOXYLIC ACID 4-Bromo-5-thiazolecarboxylic acid ethyl ester 2,5-Dibromo-thiazole-4-carboxylic acid ethyl ester 2-Bromo-4-methyl-1,3-thiazole-5-carboxylic acid Bromine 2,5-DIBROMO-THIAZOLE-4-CARBOXYLIC ACID