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2-Methyl-1,3-thiazole-4-carboxylic acid

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Products Intro: Product Name:2-Methyl-1,3-thiazole-4-carboxylic acid
CAS:35272-15-2
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2-Methyl-1,3-thiazole-4-carboxylic acid manufacturers

2-Methyl-1,3-thiazole-4-carboxylic acid Basic information
Product Name:2-Methyl-1,3-thiazole-4-carboxylic acid
Synonyms:RARECHEM AL BO 0660;CHEMBRDG-BB 4400182;BUTTPARK 98\06-12;2-METHYL-1,3-THIAZOLE-4-CARBOXYLIC ACID;2-METHYL-THIAZOLE-4-CARBOXYLIC ACID;2-Methyl-Thiazole-4-Carboxylic;2-Methyl-1,3-thiazole-4-carboxylic acid ,97%;2-Methyl-4-thiazolecarboxylic Acid
CAS:35272-15-2
MF:C5H5NO2S
MW:143.16
EINECS:233-305-4
Product Categories:Carboxylic Acids;Thiazoles, Isothiazoles &Benzothiazoles;Thiazole;Carboxylic Acids;Thiazoles, Isothiazoles & Benzothiazoles;Building Blocks
Mol File:35272-15-2.mol
2-Methyl-1,3-thiazole-4-carboxylic acid Structure
2-Methyl-1,3-thiazole-4-carboxylic acid Chemical Properties
Melting point 148 °C
Boiling point 301.2±15.0 °C(Predicted)
density 1.418±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form powder to crystal
pka4.28±0.10(Predicted)
color White to Light yellow
CAS DataBase Reference35272-15-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 2
HazardClass IRRITANT
HS Code 29341000
MSDS Information
2-Methyl-1,3-thiazole-4-carboxylic acid Usage And Synthesis
Chemical PropertiesWhite to orange to tan solid
Synthesis
	Ethyl 2-methylthiazole-4-carboxylate

6436-59-5

2-Methyl-1,3-thiazole-4-carboxylic acid

35272-15-2

The general procedure for the synthesis of 2-methyl-4-thiazolecarboxylic acid using ethyl 2-methylthiazole-4-carboxylate as starting material is as follows: 1. dissolve ethyl 2-methylthiazole-4-carboxylate in tetrahydrofuran (THF). 2. add 10% (w/v) aqueous solution of potassium hydroxide (KOH) to the above solution. 3. The reaction mixture was stirred at room temperature until thin layer chromatography (TLC) showed complete disappearance of the raw material. 4. pH of the reaction solution was adjusted to 4 with 1 M hydrochloric acid (HCl). 5. The reaction solution was extracted with ethyl acetate (EtOAc). 6. 6. The organic phase was dried with anhydrous magnesium sulfate (MgSO?). 7. The organic phase was concentrated to give the target product 2-methyl-4-thiazolecarboxylic acid.

References[1] European Journal of Medicinal Chemistry, 2017, vol. 126, p. 776 - 788
[2] Patent: US2007/105891, 2007, A1. Location in patent: Page/Page column 10
[3] Patent: US2006/160857, 2006, A1. Location in patent: Page/Page column 31
[4] Chemistry of Heterocyclic Compounds, 2011, vol. 47, # 6, p. 703 - 709
[5] Patent: WO2004/58702, 2004, A2. Location in patent: Page 29; 23
2-Methyl-1,3-thiazole-4-carboxylic acid Preparation Products And Raw materials
Raw materialsEthanol-->Ethyl acetate-->Potassium hydroxide-->Ethyl bromopyruvate-->Thioacetamide--> Ethyl 2-methylthiazole-4-carboxylate-->Water-->Tetrahydrofuran
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