2-Bromo-4-thiazolecarboxylic acid
2-Bromo-4-thiazolecarboxylic acid Basic information
- Product Name:
- 2-Bromo-4-thiazolecarboxylic acid
- Synonyms:
-
- 2-BROMOTHIAZOLE-4-CARBOXYLIC ACID
- 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 >
- CAS:
- 5198-88-9
- MF:
- C4H2BrNO2S
- MW:
- 208.03
- 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
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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
- form
- powder to crystal
- pka
- 3.13±0.10(Predicted)
- 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)
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Safety Information
- Hazard Codes
- Xi
- WGK Germany
- 3
- Hazard Note
- Irritant
- HS Code
- 29341000
- Storage Class
- 11 - Combustible Solids
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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
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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
- 2,5-DIBROMO-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER
- Methyl 2-bromothiazole-5-carboxylate
- 5-Thiazolecarboxylic acid, 2,4-dibromo-
- Ethyl 2-bromothiazole-4-carboxylate
- 2-BROMO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLIC ACID
- Ethyl 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
- Bromine
- 2-Bromo-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid