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63986-20-9

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63986-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63986-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,8 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63986-20:
(7*6)+(6*3)+(5*9)+(4*8)+(3*6)+(2*2)+(1*0)=159
159 % 10 = 9
So 63986-20-9 is a valid CAS Registry Number.

63986-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name HCl·H-Tyr(OH)-Gly-Gly-Phe-Leu-OH

1.2 Other means of identification

Product number -
Other names (Leu-enkephalin HCl)

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:63986-20-9 SDS

63986-20-9Downstream Products

63986-20-9Relevant articles and documents

An improved soluble polynorbornene support for peptide synthesis

Naganna, Nimmashetti,Madhavan, Nandita

, p. 93027 - 93031 (2015)

Soluble polymers that can be readily isolated via precipitation and possess multiple amino acid attachment sites are highly attractive for peptide synthesis. Polyethylene glycol supports that solubilize the growing peptide chain and can be readily isolated have been widely used for peptide synthesis. However, a stoichiometric amount of the PEG support is required because each PEG support typically has a single attachment site for peptide synthesis. Reported herein is the development of a polynorbornene support containing multiple attachment sites as well as alkyl and oligoether solubilizing/spacer groups. The attachment site is connected to the polymer backbone through a solubilizing oligoether linker. The support was developed after evaluating the effect of the linker and attachment site-spacing on peptide synthesis using suitably designed polynorbornene supports. The high solubility of the support minimizes the equivalents of reagents used for peptide synthesis. The support has been used to synthesize the natural product Leu5-enkephalin in 52% overall yield using only 1.2 equivalents of coupling reagents, which is comparable or superior to reported procedures using a large excess of reagents.

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