4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID

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CAS:33763-20-1
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4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID manufacturers

4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID Basic information
Product Name:4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID
Synonyms:4-METHYL-2-PHENYL-THIAZOLE-5-CARBOXYLIC ACID;4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID;AKOS BBS-00004452;IFLAB-BB F1912-0027;4-Methyl-2-phenyl-5-thiazolecarboxylicacid;4-Methyl-2-phenyl-1,3-thiazole-5-carboxylic acid, Tech.;5-Carboxy-2-phenylthiazole;2-Phenyl-4-methyl-5-thiazolecarboxylic acid
CAS:33763-20-1
MF:C11H9NO2S
MW:219.26
EINECS:
Product Categories:
Mol File:33763-20-1.mol
4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID Structure
4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID Chemical Properties
Melting point 210-212°C
Boiling point 424.0±37.0 °C(Predicted)
density 1.319±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka1.20±0.37(Predicted)
AppearanceWhite to off-white Solid
CAS DataBase Reference33763-20-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-26-36/37/39
HazardClass IRRITANT
HS Code 29349990
MSDS Information
4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID Usage And Synthesis
Chemical PropertiesWhite solid
Uses4-Methyl-2-phenyl-1,3-thiazole-5-carboxylic Acid is a useful reagent in Pd-catalyzed decarboxylative C-H cross-coupling of oxazoles and thiazoles.
Synthesis
ETHYL 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLATE

53715-64-3

4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID

33763-20-1

General method: 2N aqueous sodium hydroxide solution was slowly added to a methanol solution containing ethyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate (1 eq.) at room temperature. The reaction mixture was stirred continuously for 4 hours at room temperature. After completion of the reaction, the methanol solvent was removed by rotary evaporator. Subsequently, the pH of the reaction mixture was adjusted to 5-6 with 1N hydrochloric acid solution.The precipitated white solid was collected by filtration and processed by drying to finally give 4-methyl-2-phenylthiazole-5-carboxylic acid (1a-i).

References[1] Journal of Medicinal Chemistry, 2007, vol. 50, # 4, p. 685 - 695
[2] European Journal of Medicinal Chemistry, 2017, vol. 137, p. 96 - 107
[3] Justus Liebigs Annalen der Chemie, 1974, p. 1195 - 1205
[4] Heterocycles, 2014, vol. 89, # 2, p. 453 - 464
[5] Molecules, 2014, vol. 19, # 7, p. 9240 - 9256
Tag:4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID(33763-20-1) Related Product Information
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