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116939-85-6

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116939-85-6 Usage

General Description

BOC-MET-PRO-OH is a chemical compound consisting of a BOC-protected methionine (MET) and proline (PRO) linked to an alcohol group (OH). BOC, or t-butoxycarbonyl, is a protecting group commonly used in organic synthesis to protect sensitive functional groups from unwanted reactions. Methionine is an essential amino acid known for its antioxidant properties and plays a vital role in protein synthesis and metabolism. Proline is a non-essential amino acid that is important for the structure and function of proteins. The addition of the alcohol group adds flexibility for further chemical modifications or reactions. BOC-MET-PRO-OH can be used as a building block in peptide synthesis or as a precursor for the synthesis of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 116939-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,9,3 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116939-85:
(8*1)+(7*1)+(6*6)+(5*9)+(4*3)+(3*9)+(2*8)+(1*5)=156
156 % 10 = 6
So 116939-85-6 is a valid CAS Registry Number.

116939-85-6SDS

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 (2S)-1-[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoyl]pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names N-Boc-L-Met-L-Pro-OH

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:116939-85-6 SDS

116939-85-6Relevant articles and documents

A copper-catalyzed, pH-neutral construction of high-enantiopurity peptidyl ketones from peptidic S-acylthiosalicylamides in air at room temperature

Liebeskind, Lanny S.,Yang, Hao,Li, Hao

supporting information; body text, p. 1417 - 1421 (2009/07/18)

A copper-catalyzed transformation of peptidic thiol esters and boronic acids gives peptidyl ketones and takes place in DMF or DMF/H2O at room temperature in air (see scheme). This aerobic reaction only occurs at a thiol ester group capable of coordinating

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