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Nα-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid

Base Information Edit
  • Chemical Name:Nα-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid
  • CAS No.:108460-09-9
  • Molecular Formula:C26H28N4O6S
  • Molecular Weight:524.598
  • Hs Code.:
  • Mol file:108460-09-9.mol
N<sub>α</sub>-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid

Synonyms:Nα-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid

Suppliers and Price of Nα-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Nα-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid Edit
Chemical Property:
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MSDS Files:

SDS file from LookChem

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Technology Process of Nα-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid

There total 3 articles about Nα-(2-Naphthylsulfonylglycyl)-4-nitro-phenylalaninpiperidid 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: 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
With N-ethylmorpholine;; sodium hydroxide; chlorocarbon isobutylester; In ethyl acetate;
Guidance literature:
Multi-step reaction with 2 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
With N-ethylmorpholine;; sodium hydroxide; chlorocarbon isobutylester; In ethyl acetate;
Guidance literature:
With N-ethylmorpholine;; chlorocarbon isobutylester; Yield given. Multistep reaction; 1.) acetic ester, 25 min; 2.) 4 h, room temperature;
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