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4-Isothiazolecarboxylic acid, 3-Methyl-, Methyl ester

Base Information
  • Chemical Name:4-Isothiazolecarboxylic acid, 3-Methyl-, Methyl ester
  • CAS No.:74410-97-2
  • Molecular Formula:C6H7NO2S
  • Molecular Weight:157.193
  • Hs Code.:
  • Mol file:74410-97-2.mol
4-Isothiazolecarboxylic acid, 3-Methyl-, Methyl ester

Synonyms:

Suppliers and Price of 4-Isothiazolecarboxylic acid, 3-Methyl-, Methyl ester
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Matrix Scientific
  • Methyl 3-methylisothiazole-4-carboxylate
  • 500mg
  • $ 315.00
  • Crysdot
  • Methyl3-methylisothiazole-4-carboxylate 97%
  • 1g
  • $ 356.00
  • CHESS?
  • KF000977:3-Methyl-isothiazole-4-carboxylicacidmethylester 98
  • 1 g
  • $ 336.00
Total 19 raw suppliers
Chemical Property of 4-Isothiazolecarboxylic acid, 3-Methyl-, Methyl ester
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

Methyl 3-methylisothiazole-4-carboxylate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Methyl 3-Methylisothiazole-4-carboxylate is used in preparation of substituted fused pyrimidinamines as PI3 kinase modulators useful in treating cancer.
Technology Process of 4-Isothiazolecarboxylic acid, 3-Methyl-, Methyl ester

There total 11 articles about 4-Isothiazolecarboxylic acid, 3-Methyl-, Methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 3-chloro-benzenecarboperoxoic acid; In ethanol; at 70 ℃; for 3h;
DOI:10.1039/P19890001241
Guidance literature:
methyl 3-amino-2-thioformylbut-2-enoate; With 3-chloro-benzenecarboperoxoic acid; In ethanol; for 3h; under 760.051 Torr; Reflux;
With sodium hydroxide; In ethanol; water; at 20 ℃; under 760.051 Torr;
Guidance literature:
Multi-step reaction with 2 steps
1.1: trichlorophosphate / tetrahydrofuran / 0 - 30 °C / 760.05 Torr
1.2: 760.05 Torr
2.1: 3-chloro-benzenecarboperoxoic acid / ethanol / 3 h / 760.05 Torr / Reflux
2.2: 20 °C / 760.05 Torr
With 3-chloro-benzenecarboperoxoic acid; trichlorophosphate; In tetrahydrofuran; ethanol;
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