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1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone

Base Information
  • Chemical Name:1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone
  • CAS No.:1039757-81-7
  • Molecular Formula:C12H13NOS2
  • Molecular Weight:251.373
  • Hs Code.:
  • Mol file:1039757-81-7.mol
1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone

Synonyms:1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone

Suppliers and Price of 1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone
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
  • JR MediChem
  • 1-Propanone,1-[(4S)-4-phenyl-2-thioxo-3-thiazolidinyl]- 96%
  • 1g
  • $ 398.00
Total 6 raw suppliers
Chemical Property of 1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone
Chemical Property:
  • PSA:77.70000 
  • LogP:2.93590 
Purity/Quality:

NLT 98% *data from raw suppliers

1-Propanone,1-[(4S)-4-phenyl-2-thioxo-3-thiazolidinyl]- 96% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone

There total 4 articles about 1-[(4R)-4-phenyl-2-thioxo-3-thiazolidinyl]-1-Propanone 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 sodium hydride; In tetrahydrofuran; mineral oil; at 78 ℃; Inert atmosphere;
DOI:10.1080/10426507.2014.931399
Guidance literature:
With 2-chloro-1-methylpyridinium p-toluenesulfonate; triethylamine; In dichloromethane; at 25 ℃; for 5h; Reagent/catalyst;
Guidance literature:
With 2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine; N-ethyl-N,N-diisopropylamine; In chloroform-d1; at 25 ℃; for 1.5h; Inert atmosphere;
DOI:10.1021/ol303239t
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