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Cbz-4-Nitro-D-Phenylalanine is a chemical compound that belongs to the class of amino acids, specifically a derivative of phenylalanine with a 4-nitrobenzyl group and a carboxybenzyl (Cbz) protecting group. It is commonly used in pharmaceutical and organic chemistry due to its unique structure and properties, making it a valuable component in drug development and research.

117402-88-7

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117402-88-7 Usage

Uses

Used in Pharmaceutical Industry:
Cbz-4-Nitro-D-Phenylalanine is used as a building block for the synthesis of peptide-based pharmaceuticals, contributing to the development of new drugs with specific therapeutic properties.
Used in Organic Chemistry:
Cbz-4-Nitro-D-Phenylalanine serves as a key intermediate in the production of various pharmaceuticals and agrochemicals, facilitating the creation of compounds with targeted applications in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 117402-88-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,4,0 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117402-88:
(8*1)+(7*1)+(6*7)+(5*4)+(4*0)+(3*2)+(2*8)+(1*8)=107
107 % 10 = 7
So 117402-88-7 is a valid CAS Registry Number.

117402-88-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name D-Z-4-NO2-Phe-OH

1.2 Other means of identification

Product number -
Other names Cbz-4-Nitro-D-Phenylalanine

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:117402-88-7 SDS

117402-88-7Downstream Products

117402-88-7Relevant academic research and scientific papers

PAPAIN-ASSISTED RESOLUTION OF NATURAL AND XENOBIOTIC α-AMINO ACIDS

Moriniere, J. L.,Danree, B.,Lemoine, J.,Guy, A.

, p. 441 - 444 (2007/10/02)

A new and convenient method for the preparation of pure enantiomers of α-amino acids is described.Industrial papain, catalyzes the synthesis of L-Z-amino acid ethyl esters in ethanolic medium, with good yields.These esters are obtained from DL-Z-amino acids with 100percent optical purity.Unreactive D-Z-amino acids are readily isolated from reaction medium.Physical constants of natural and xenobiotic L-Z-amino acid esters and D-Z-amino acids are described.

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