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4-Thiazolecarboxylic acid

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CAS:3973-08-8
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CAS:3973-08-8
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4-Thiazolecarboxylic acid Basic information
Product Name:4-Thiazolecarboxylic acid
Synonyms:4-Thiazolecarboxylic acid 3973-8-8;1,3-Thiazole-4-Carboxylic Acid 3973-8-8;1,3-thiazole-4-carboxylic acid(SALTDATA: FREE);4-Carboxy-1,3-thiazole;NSC 195467;4-Thiazolecarboxylic acid 97%;4-Thiazolecarboxylic Acid, 97+%;3973/8/8
CAS:3973-08-8
MF:C4H3NO2S
MW:129.14
EINECS:628-056-7
Product Categories:Carboxylic Acids;Thiazoles, Isothiazoles & Benzothiazoles;Thiazoles;Sulphur Derivatives;Carboxylic Acids;Thiazoles, Isothiazoles &Benzothiazoles;Heterocycles;Miscellaneous Reagents;Sulfur & Selenium Compounds;Building Blocks;Heterocyclic Building Blocks;blocks;Carboxes;bc0001
Mol File:3973-08-8.mol
4-Thiazolecarboxylic acid Structure
4-Thiazolecarboxylic acid Chemical Properties
Melting point 195-199 °C (lit.)
Boiling point 191 °C
density 1.525±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka3.57±0.10(Predicted)
color White to Off-White
λmax230nm(EtOH)(lit.)
InChIInChI=1S/C4H3NO2S/c6-4(7)3-1-8-2-5-3/h1-2H,(H,6,7)
InChIKeyHMVYYTRDXNKRBQ-UHFFFAOYSA-N
SMILESS1C=C(C(O)=O)N=C1
CAS DataBase Reference3973-08-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 43
Safety Statements 36/37
WGK Germany 3
HazardClass IRRITANT
HS Code 29341000
Storage Class11 - Combustible Solids
Hazard ClassificationsSkin Sens. 1
MSDS Information
ProviderLanguage
SigmaAldrich English
4-Thiazolecarboxylic acid Usage And Synthesis
Chemical PropertiesPale yellow to white solid
Uses4-Thiazolecarboxylic Acid (cas# 3973-08-8) is a compound useful in organic synthesis.
Synthesis
4-Methylthiazole

693-95-8

4-Thiazolecarboxylic acid

3973-08-8

The general procedure for the synthesis of thiazole-4-carboxylic acid from 4-methylthiazole was as follows: 4-methylthiazole (19.8 g, 0.2 mol), 200 mL of water, and potassium permanganate (173.8 g, 1.1 mol) were added to a 500 mL three-necked flask, which was heated to 55 °C with stirring and kept for 22 hours. After completion of the reaction, the reaction mixture was cooled and filtered. The filter cake (mainly composed of manganese dioxide) was washed with hot water at 50°C. The filtrate was adjusted to pH 3 with dilute hydrochloric acid, precipitated as a solid and filtered. The filter cake was washed with a small amount of water and dried to give 18.1 g of thiazole-4-carboxylic acid in 70.2% yield, melting point 196-198 °C.

References[1] Angewandte Chemie, 1992, vol. 104, # 6, p. 748 - 749
[2] Patent: CN104557902, 2018, B. Location in patent: Paragraph 0063; 0076; 0081; 0088; 0089; 0102
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