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131068-47-8

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131068-47-8 Usage

General Description

SUC-ALA-ALA-PRO-ARG-PNA is a chemical compound composed of the amino acids alanine, proline, and arginine, as well as the compound SUC, which refers to succinyl, a type of ester. These amino acids are essential for building proteins and are involved in various physiological processes in the body. SUC-ALA-ALA-PRO-ARG-PNA may have potential use in pharmaceutical research or drug development due to its unique composition and potential biological activity. Further studies are needed to fully understand the properties and potential applications of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 131068-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,6 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131068-47:
(8*1)+(7*3)+(6*1)+(5*0)+(4*6)+(3*8)+(2*4)+(1*7)=98
98 % 10 = 8
So 131068-47-8 is a valid CAS Registry Number.

131068-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Suc-AAPR-pNA

1.2 Other means of identification

Product number -
Other names 10006 SUC-ALA-ALA-PRO-ARG-PNA

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:131068-47-8 SDS

131068-47-8Upstream product

131068-47-8Downstream Products

131068-47-8Relevant articles and documents

Solid phase synthesis of peptide para-nitroanilides

Burdick,Struble,Burnier

, p. 2589 - 2592 (2007/10/02)

A facile synthesis of peptide para-nitroanilides was developed using a novel urethane linked para-aminoanilide resin 3 and solid phase peptide synthesis. Conversion of the resulting peptide para-aminoanilides to the corresponding peptide para-nitroanilides was achieved by oxidation with sodium perborate. With the exception of sequences containing methionine, tryptophan and cysteine, all amino acid residues can be used. A representative synthesis of the tetrapeptide para-nitroanilide succinyl-Ala-Ala-Pro-Arg-PNA is described.

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