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Boc-Tyr(Cl2Bzl)-Gly-Gly-Phe-Met-OBzl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129398-68-1

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129398-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129398-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,9 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129398-68:
(8*1)+(7*2)+(6*9)+(5*3)+(4*9)+(3*8)+(2*6)+(1*8)=171
171 % 10 = 1
So 129398-68-1 is a valid CAS Registry Number.

129398-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Tyr(Cl2Bzl)-Gly-Gly-Phe-Met-OBzl

1.2 Other means of identification

Product number -
Other names -

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:129398-68-1 SDS

129398-68-1Downstream Products

129398-68-1Relevant academic research and scientific papers

Sulphur Trioxide/Thiol: A Novel System for the Reduction of Methionine Sulphoxide

Futaki, Shiroh,Yagami, Takeshi,Taike, Takashi,Akita, Tadashi,Kitagawa, Kouki

, p. 653 - 658 (2007/10/02)

A new method for the effective reduction of methionine sulphoxide in protected peptides with sulphur trioxide and thiol has been developed.In practice, a combination of dimethylformamide-sulphur trioxide complex and ethane-1,2-dithiol was found effective, the presence of pyridine in the reaction medium being found necessary for the reduction to proceed.Methionine sulphoxide in two types of protected methionine-enkephalins was efficiently reduced to methionine by this reduction system at 20 deg C in an hour.The (p-methylsulphinyl)benzyl protecting group was also reduced to (p-methylthio)benzyl simultaneously with the reduction of methionine sulphoxide.Subsequent deprotection afforded methionine-enkephalin of high purity in each case.

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