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72636-02-3

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72636-02-3 Usage

General Description

VAL-THR, also known as valine-threonine, is a dipeptide composed of two amino acids, valine and threonine. Valine is a branched-chain amino acid that is important for muscle metabolism and energy production. It is also involved in the maintenance and repair of tissues. Threonine is an essential amino acid that plays a key role in protein synthesis, immune function, and the maintenance of healthy skin and teeth. Together, VAL-THR serves as a source of these important amino acids, supporting various biological functions including muscle development, tissue repair, and overall health.

Check Digit Verification of cas no

The CAS Registry Mumber 72636-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,3 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72636-02:
(7*7)+(6*2)+(5*6)+(4*3)+(3*6)+(2*0)+(1*2)=123
123 % 10 = 3
So 72636-02-3 is a valid CAS Registry Number.

72636-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name L-valyl-L-threonine

1.2 Other means of identification

Product number -
Other names (S)-(-)-3-(Benzoylthio)-2-methylpropanoic acid

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:72636-02-3 SDS

72636-02-3Downstream Products

72636-02-3Relevant articles and documents

Synthesis of dipeptides based on valine and threonine

Sorokina, Yu. M.,Sladkova,Popova,Shadyro,Knizhnikov

, p. 1297 - 1301 (2012)

Val-Val, Val-Thr, and Thr-Val dipeptides were synthesized using trifluoroacetyl protecting group. The optical rotations of the products were similar to those of samples synthesized using Boc protection, which indicated the absence of racemization in the course of introduction and removal of trifluoroacetyl protection. Pleiades Publishing, Ltd., 2012.

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