4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID

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Products Intro: Product Name:4-Bromo-1,3-thiazole-2-carboxylic acid
CAS:88982-82-5
Purity:99% Package:100kg;1.6USD|10kg;3.6USD|1kg;6.6USD
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Products Intro: Product Name:4-Bromothiazole-2-carboxylic Acid
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Products Intro: Product Name:4-Bromo-1,3-thiazole-2-carboxylic acid
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4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID manufacturers

4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID Basic information
Product Name:4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID
Synonyms:4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID;4-BROMO-2-THIAZOLE CARBOXYLIC ACID;4-BROMO-THIAZOLE-2-CARBOXYLIC ACID;4-BROMO-1,3-THIAZOLE-2-CA...;2-Thiazolecarboxylicacid,4-broMo;4-Bromo-1,3-thiazole-2-carboxylic acid 96%;3-THIAZOLE-2-CARBOXYLIC ACID;4-Bromo-thiazol-2-carboxylic acid
CAS:88982-82-5
MF:C4H2BrNO2S
MW:208.03
EINECS:
Product Categories:
Mol File:88982-82-5.mol
4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID Structure
4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID Chemical Properties
Boiling point 372.5±34.0 °C(Predicted)
density 2.062±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka2.53±0.10(Predicted)
AppearanceLight yellow to light brown Solid
InChIInChI=1S/C4H2BrNO2S/c5-2-1-9-3(6-2)4(7)8/h1H,(H,7,8)
InChIKeyAYUAEJPYEJEHJN-UHFFFAOYSA-N
SMILESS1C=C(Br)N=C1C(O)=O
CAS DataBase Reference88982-82-5
Safety Information
HazardClass IRRITANT
HS Code 2934208090
MSDS Information
4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID Usage And Synthesis
Synthesis
Carbon dioxide

124-38-9

2,4-Dibromothiazole

4175-77-3

4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID

88982-82-5

To a solution of 2,4-dibromothiazole (50 g, 207 mmol, 1.0 eq.) in anhydrous ether (1000 ml) was slowly added n-butyllithium (90 ml, 2.5 M, 1.1 eq.) dropwise at -78 °C. The temperature was maintained at -78 °C and the reaction mixture was stirred for 1 hour. Subsequently, the reaction solution was poured into dry carbon dioxide at the same temperature and the reaction mixture was gradually warmed up to room temperature. The completion of the reaction was confirmed by monitoring the progress of the reaction by thin layer chromatography (TLC) and liquid chromatography-mass spectrometry (LCMS). After completion of the reaction, the reaction was quenched with deionized water (100 ml). The ether phase was separated and discarded. The aqueous phase was adjusted to pH 2-3 with dilute hydrochloric acid and then extracted with ethyl acetate. The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 35 g of 4-bromo-1,3-thiazole-2-carboxylic acid in 82% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.23 (1H, s).

References[1] Patent: US2014/179663, 2014, A1. Location in patent: Paragraph 0174
[2] Journal of Fluorine Chemistry, 1991, vol. 55, # 2, p. 173 - 178
[3] Patent: WO2008/57336, 2008, A2. Location in patent: Page/Page column 36
[4] Patent: US2015/175597, 2015, A1. Location in patent: Paragraph 0179; 0180
4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materialsETHYL 4-BROMOTHIAZOLE-2-CARBOXYLATE-->Carbon dioxide-->2,4-Dibromothiazole-->n-Butyllithium-->Diethyl ether
Tag:4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID(88982-82-5) Related Product Information
ETHYL 4-BROMOTHIAZOLE-2-CARBOXYLATE (4-BROMO-THIAZOL-2-YL)-METHANOL 4-BROMO-1,3-THIAZOLE-2-CARBOXYLIC ACID 4-BROMO-2-METHYLTHIAZOLE 4-BROMO-2-FORMYLTHIAZOLE

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