Thiazole-2-carboxylic acid

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Thiazole-2-carboxylic acid manufacturers

Thiazole-2-carboxylic acid Basic information
Product Name:Thiazole-2-carboxylic acid
Synonyms:1,3-THIAZOLE-2-CARBOXYLIC ACID;RARECHEM AL BE 0750;2-THIAZOLECARBOXYLIC ACID,THIAZOLE-2-CARBOXYLIC ACID;Thiazole-2-carboxylic acid ,98%;2-THIAZOLECARBOXYLIC;2-Carboxy-1,3-thiazole;thiazol-2-carboxylic acid;Thiazole-2-carboxylic acid
CAS:14190-59-1
MF:C4H3NO2S
MW:129.14
EINECS:
Product Categories:Carboxylic Acids;Thiazoles, Isothiazoles & Benzothiazoles;Carboxylic Acids;Thiazoles, Isothiazoles &Benzothiazoles;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Thiazole series
Mol File:14190-59-1.mol
Thiazole-2-carboxylic acid Structure
Thiazole-2-carboxylic acid Chemical Properties
Melting point 91.6-93°C
Boiling point 310.6±25.0 °C(Predicted)
density 1.525±0.06 g/cm3(Predicted)
storage temp. -20°C
pka2.95±0.10(Predicted)
form Solid
AppearanceWhite to off-white Solid
Water Solubility Slightly soluble in water.
InChI1S/C4H3NO2S/c6-4(7)3-5-1-2-8-3/h1-2H,(H,6,7)
InChIKeyIJVLVRYLIMQVDD-UHFFFAOYSA-N
SMILESOC(=O)c1nccs1
CAS DataBase Reference14190-59-1(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38-22
Safety Statements 26-36/37/39-22
WGK Germany 1
HS Code 29349990
Storage Class11 - Combustible Solids
MSDS Information
Thiazole-2-carboxylic acid Usage And Synthesis
Chemical PropertiesBeige to light yellow powder
UsesThiazole-2-carboxylic acid is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
Synthesis
Ethyl thiazole-2-carboxylate

14527-42-5

THIAZOLE-2-CARBOXYLIC ACID

14190-59-1

General procedure for the synthesis of thiazole-2-carboxylic acid from ethyl 2-thiazolecarboxylate: 2N aqueous KOH solution (3.5 mL, 5 eq.) was added to a solution of ethyl 2-thiazolecarboxylate (213 mg, 1.355 mmol) in ethanol (3 mL) at 116 °C. The reaction mixture was stirred at room temperature for 2 hours and then acidified with 2N HCl (3.5 mL). The acidified mixture was allowed to stand overnight and needle-like crystals were precipitated and collected by filtration to give thiazole-2-carboxylic acid (43.3 mg, 25% yield).

References[1] Patent: US2007/185056, 2007, A1. Location in patent: Page/Page column 49
[2] Helvetica Chimica Acta, 1945, vol. 28, p. 924
[3] Patent: WO2008/76243, 2008, A2. Location in patent: Page/Page column 75
[4] Patent: WO2008/85316, 2008, A1. Location in patent: Page/Page column 73
[5] Patent: WO2006/138373, 2006, A2. Location in patent: Page/Page column 128-129
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