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20582-55-2

Ethyl 4-methylthiazole-5-carboxylate

CAS: 20582-55-2

Molecular Formula: C7H9NO2S

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20582-55-2 - Names and Identifiers

Name Ethyl 4-methylthiazole-5-carboxylate
Synonyms ETHYL 4-METHYL-5-THIAZOLEACTATE
Ethyl 4-methyl-5-thiazoleactate
Ethyl 4-methyl-5-thiazoly formate
Ethyl 4-methyl-5-thiazolyl formate
ETHYL 4-METHYL-5-THIAZOLYL FORMATE
ETHYL 4-METHYL-5-THIAZOLECARBOXYLATE
Ethyl 4-methylthiazole-5-carboxylate
ETHYL 4-METHYLTHIAZOLE-5-CARBOXYLATE
Ethyl-4-methyl-5-thizaolecarboxylate
ethyl 4-methyl-1,3-thiazole-5-carboxylate
4-Methyl-5-Thiazolecarboxylic Acid Ethyl Ester
5-THIAZOLECARBOXYLIC ACID, 4-METHYL-, ETHYL ESTER
CAS 20582-55-2
InChI InChI=1/C8H11NO4S/c1-3-13-7(10)6-5(2)4-14-9(6)8(11)12/h4,6H,3H2,1-2H3,(H,11,12)

20582-55-2 - Physico-chemical Properties

Molecular FormulaC7H9NO2S
Molar Mass171.22
Density1.198±0.06 g/cm3(Predicted)
Melting Point28°C(lit.)
Boling Point233°C(lit.)
AppearanceWhite to light yellow crystal powder
pKa1.57±0.10(Predicted)
Storage ConditionKeep in dark place,Sealed in dry,Room Temperature
Refractive Index1.571

20582-55-2 - Risk and Safety

Hazard ClassIRRITANT

20582-55-2 - Reference Information

introduction ethyl 4-methylthiazol-5-formate is carboxylate organic matter, density: 1.198
g/cm3, boiling point: 239.1°C at 760 mmHg, white to light yellow crystal powder.
Uses Ethyl 4-methylthiazol-5-formate is a key intermediate for the synthesis of ceftorenpivoxil (Cefditoren pivoxil). Cefditoren pivoxil was developed by Meiji Fruit Company of Japan and was listed in Japan under the trade name of Meiact in 1994. Cefitorenpiproxil has a broad antibacterial spectrum against Gram-positive and Gram-negative bacteria.
synthesis method we have designed a new process for synthesizing ethyl 4-methylthiazol-5-formate with ethyl 2-chloroacetoacetate as starting material. its main characteristics are as follows:(1) using ammonium thiocyanate and ethyl 2-chloroacetoacetate to prepare ethyl 4-methylthiazol-5-formate, the problems of low yield, complex operation and large amount of waste liquid caused by diazotization reaction and multi-step reaction in the traditional process are avoided;(2) Solvent-free reaction is realized, which greatly simplifies the solvent recovery and treatment process and reduces the cost. The specific synthesis route is as follows:
Last Update:2024-04-10 22:29:15
20582-55-2
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CAS: 20582-55-2
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
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Shanghai Amole Biotechnology Co., Ltd.
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CAS: 20582-55-2
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365 Click to send a QQ message
Wechat: 18916960931
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
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Product Name: Ethyl 4-methylthiazole-5-carboxylate Visit Supplier Webpage Request for quotation
CAS: 20582-55-2
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
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Product Name: Ethyl 4-Methylthiazole-5-carboxylate Visit Supplier Webpage Request for quotation
CAS: 20582-55-2
Tel: +86 0571-86722205
Email: sales@chinaskyrun.com
Mobile: +8618958170122
QQ: 2531159185 Click to send a QQ messageSend QQ message
Wechat: chinaskyrun
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: Ethyl4-Methyl-5-Thiazoleactate Visit Supplier Webpage Request for quotation
CAS: 20582-55-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
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