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69901-75-3

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69901-75-3 Usage

Chemical Properties

Cbz-Cyclohexyl-L-glycine is white to Off-White Solid

Uses

Different sources of media describe the Uses of 69901-75-3 differently. You can refer to the following data:
1. Cbz-Cyclohexyl-L-glycine is a gylicine derivative used in the preparation of peptides as inhibitors of serine proteases, particularly hepatitis C virus NS3-NS4A protease.
2. A gylicine derivative used in the preparation of peptides as inhibitors of serine proteases, particularly hepatitis C virus NS3-NS4A protease.

Check Digit Verification of cas no

The CAS Registry Mumber 69901-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69901-75:
(7*6)+(6*9)+(5*9)+(4*0)+(3*1)+(2*7)+(1*5)=163
163 % 10 = 3
So 69901-75-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO4/c18-15(19)14(13-9-5-2-6-10-13)17-16(20)21-11-12-7-3-1-4-8-12/h1,3-4,7-8,13-14H,2,5-6,9-11H2,(H,17,20)(H,18,19)/t14-/m0/s1

69901-75-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (H63723)  N-Benzyloxycarbonyl-L-2-cyclohexylglycine, 95%   

  • 69901-75-3

  • 5g

  • 1004.0CNY

  • Detail
  • Alfa Aesar

  • (H63723)  N-Benzyloxycarbonyl-L-2-cyclohexylglycine, 95%   

  • 69901-75-3

  • 25g

  • 1646.0CNY

  • Detail
  • Alfa Aesar

  • (H63723)  N-Benzyloxycarbonyl-L-2-cyclohexylglycine, 95%   

  • 69901-75-3

  • 100g

  • 4939.0CNY

  • Detail

69901-75-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-(((Benzyloxy)carbonyl)amino)-2-cyclohexylacetic acid

1.2 Other means of identification

Product number -
Other names (2S)-2-cyclohexyl-2-(phenylmethoxycarbonylamino)acetic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69901-75-3 SDS

69901-75-3Relevant articles and documents

PROCESS FOR PRODUCING N-PROTECTED AMINO ACID

-

Page/Page column 3, (2011/07/06)

The present invention relates to a method for producing N-protected amino acid. Specifically, the present invention provides a method in which a protecting group is introduced to the amino group of an amino acid in a reaction under alkaline condition, and the N-protected amino acid thus generated is then separated from the reaction solution as crystals, without undergoing an extraction step or a concentration step. The present inventors have completed the invention based on the finding that desirable crystals of N-protected amino acids may be obtained without extraction, concentration or recrystallization steps between the initial generation of the N-protected amino acid molecules and the subsequent separation of the crystals, by first adding an water-soluble organic solvent and optionally water to the reaction solution (alkaline) containing the N-protected amino acid, and then neutralizing the solution by an acid.

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