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N-alpha-(2-naphthylsulfonylglycyl)-1-(4-aminophenylalanine)piperidide

Base Information Edit
  • Chemical Name:N-alpha-(2-naphthylsulfonylglycyl)-1-(4-aminophenylalanine)piperidide
  • CAS No.:108460-12-4
  • Molecular Formula:C26H30N4O4S
  • Molecular Weight:494.615
  • Hs Code.:
  • Mol file:108460-12-4.mol
N-alpha-(2-naphthylsulfonylglycyl)-1-(4-aminophenylalanine)piperidide

Synonyms:Acetamide,N-[1-[(4-aminophenyl)methyl]-2-oxo-2-(1-piperidinyl)ethyl]-2-[(2-naphthalenylsulfonyl)amino]-,(?à)-

Suppliers and Price of N-alpha-(2-naphthylsulfonylglycyl)-1-(4-aminophenylalanine)piperidide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 1 raw suppliers
Chemical Property of N-alpha-(2-naphthylsulfonylglycyl)-1-(4-aminophenylalanine)piperidide Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:133.47000 
  • Density:1.313g/cm3 
  • LogP:5.27140 
Purity/Quality:
Safty Information:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of N-alpha-(2-naphthylsulfonylglycyl)-1-(4-aminophenylalanine)piperidide

There total 5 articles about N-alpha-(2-naphthylsulfonylglycyl)-1-(4-aminophenylalanine)piperidide 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 2 steps
1: 1.) N-ethyl morpholine, chlorocarbon isobutylester / 1.) acetic ester, 25 min; 2.) 4 h, room temperature
2: NH3/hydrogen / Raney-Ni / methanol
With N-ethylmorpholine;; chlorocarbon isobutylester; ammonia; hydrogen; nickel; In methanol;
Guidance literature:
Multi-step reaction with 3 steps
1: 56 percent / aqu. NaOH / ethyl acetate / 5 h
2: 1.) N-ethyl morpholine, chlorocarbon isobutylester / 1.) acetic ester, 25 min; 2.) 4 h, room temperature
3: NH3/hydrogen / Raney-Ni / methanol
With N-ethylmorpholine;; sodium hydroxide; chlorocarbon isobutylester; ammonia; hydrogen; nickel; In methanol; ethyl acetate;
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