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(R)-(+)-p-chloro-N-acetyl-1-methylbenzylamine

Base Information Edit
  • Chemical Name:(R)-(+)-p-chloro-N-acetyl-1-methylbenzylamine
  • CAS No.:186296-21-9
  • Molecular Formula:C10H12ClNO
  • Molecular Weight:197.664
  • Hs Code.:
  • Mol file:186296-21-9.mol
(R)-(+)-p-chloro-N-acetyl-1-methylbenzylamine

Synonyms:Acetamide,N-[1-(4-chlorophenyl)ethyl]-, (R)-

Suppliers and Price of (R)-(+)-p-chloro-N-acetyl-1-methylbenzylamine
Supply Marketing:Edit
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
Total 5 raw suppliers
Chemical Property of (R)-(+)-p-chloro-N-acetyl-1-methylbenzylamine Edit
Chemical Property:
  • PSA:32.59000 
  • Density:1.136 
  • LogP:3.37740 
Purity/Quality:

98%Min *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of (R)-(+)-p-chloro-N-acetyl-1-methylbenzylamine

There total 57 articles about (R)-(+)-p-chloro-N-acetyl-1-methylbenzylamine 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 BF4; hydrogen; In tetrahydrofuran; at 5 ℃; for 0.5h; under 760 Torr;
DOI:10.1021/ja974045k
Guidance literature:
With (S)-diBr-SIPHOS; hydrogen; rhodium(I)-bis(1,5-cyclooctadiene) tetrafluoroborate; In toluene; at 0 ℃; for 30h; under 38000 Torr;
DOI:10.1016/j.tetasy.2003.08.017
Guidance literature:
With bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; C34H27F4NP2; In dichloromethane; at 20 ℃; for 24h; under 7600.51 Torr; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1002/adsc.200800418
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