Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(R)-3-chloromandelamide

Base Information Edit
  • Chemical Name:(+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(R)-3-chloromandelamide
  • CAS No.:121251-83-0
  • Molecular Formula:C18H18ClNO3
  • Molecular Weight:331.799
  • Hs Code.:
  • Mol file:121251-83-0.mol
(+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(R)-3-chloromandelamide

Synonyms:

Suppliers and Price of (+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(R)-3-chloromandelamide
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 0 raw suppliers
Chemical Property of (+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(R)-3-chloromandelamide Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(R)-3-chloromandelamide

There total 4 articles about (+)-N-<(2R)-7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl>-(R)-3-chloromandelamide 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:
Multi-step reaction with 3 steps
2: 30 percent / 1.) 48percent HBr aq., 2.) NH4OH / 3 h / Heating
3: benzotriazol-1-yloxy-tris(dimethylamino)hposphonium hexafluorophosphate, TEA / CH2Cl2 / 5 h / Ambient temperature
With ammonium hydroxide; TEA; hydrogen bromide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; In dichloromethane;
DOI:10.1016/0223-5234(94)90095-7
Guidance literature:
Multi-step reaction with 2 steps
1: 30 percent / 1.) 48percent HBr aq., 2.) NH4OH / 3 h / Heating
2: benzotriazol-1-yloxy-tris(dimethylamino)hposphonium hexafluorophosphate, TEA / CH2Cl2 / 5 h / Ambient temperature
With ammonium hydroxide; TEA; hydrogen bromide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; In dichloromethane;
DOI:10.1016/0223-5234(94)90095-7
Guidance literature:
With TEA; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; In dichloromethane; for 5h; Ambient temperature;
DOI:10.1016/0223-5234(94)90095-7
Post RFQ for Price