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amflutizole

amflutizole Suppliers list
Company Name: BOC Sciences  
Tel: 16314854226; +8616314854226
Email: inquiry@bocsci.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: Shanghai Yifei Biotechnology Co. , Ltd.  
Tel: 021-65675885 18964387627
Email: customer_service@efebio.com
Company Name: Beijing Boorsen Biotechnology Co., Ltd  
Tel: 400-901-9800 18611424007
Email: cis@bioss.com.cn
Company Name: Nanjing Shizhou Biology Technology Co.,Ltd  
Tel: 025-85560043 15850508050
Email: cindy.huang@synzest.com

amflutizole manufacturers

  • amflutizole
  • amflutizole pictures
  • $133.00
  • 2026-05-11
  • CAS:82114-19-0
  • Purity: 99.61%
  • Supply Ability: 10g
amflutizole Basic information
Product Name:amflutizole
Synonyms:amflutizole;4-Amino-3-(3-trifluoromethylphenyl)-5-isothiazolecarboxylic acid;4-Amino-3-[3-(trifluoromethyl)phenyl]-1,2-thiazole-5-carboxylic Acid;5-Isothiazolecarboxylic acid, 4-amino-3-[3-(trifluoromethyl)phenyl]-;amflutizole, 10 mM in DMSO
CAS:82114-19-0
MF:C11H7F3N2O2S
MW:288.25
EINECS:
Product Categories:
Mol File:82114-19-0.mol
amflutizole Structure
amflutizole Chemical Properties
Boiling point 332.6±42.0 °C(Predicted)
density 1.551±0.06 g/cm3(Predicted)
pka4.16±0.30(Predicted)
Safety Information
MSDS Information
amflutizole Usage And Synthesis
OriginatorLY 141894,Eli Lilly
UsesSuppressant (gout).
Manufacturing ProcessTo a stirred solution of 3-trifluoromethyl-α-(p-toluenesulfonyloxyimino) benzylcyanide in methanol containing methyl thioglycolate was added dropwise over a 30 min period triethylamine. The reaction mixture was stirred at room temperature for 4 h following complete addition, and then was cooled to 0°C and filtered. The precipitate which was collected was recrystallized from hexane and ethyl acetate to provide methyl 3-(3-trifluoromethylphenyl)- 4-amino-5-isothiazolecarboxylate, melting point 94°-95°C.
A solution of methyl 3-(3-trifluoromethylphenyl)-4-amino-5- isothiazolecarboxylate and potassium hydroxide in methanol was heated at reflux for 6 h. The reaction mixture was then poured into ice containing 12 N aqueous hydrochloric acid. The free acid precipitated from the acidic solution, and after all of the ice had melted, the aqueous acidic mixture was filtered. The precipitate was crystallized from ethanol and water to provide 3-(3- trifluoromethylphenyl)-4-amino-5-isothiazolecarboxylic acid, melting point 179°-180°C. Yield 80%.
Therapeutic FunctionUricosuric
amflutizole Preparation Products And Raw materials
Raw materialsTriethylamine-->Potassium hydroxide-->Methyl thioglycolate
Tag:amflutizole(82114-19-0) Related Product Information
5-Isothiazolecarboxylic acid Isothiazole-5-carbaldehyde 3-Methylisothiazole 4-Isothiazolamine(9CI) 3-Methylisothiazole-5-carboxylic acid amflutizole 3-(3-(Trifluoromethyl)phenyl)-5-isothiazolecarboxylic acid