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D-Valine, N-formyl-3-mercapto- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13833-89-1

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13833-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13833-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,3 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13833-89:
(7*1)+(6*3)+(5*8)+(4*3)+(3*3)+(2*8)+(1*9)=111
111 % 10 = 1
So 13833-89-1 is a valid CAS Registry Number.

13833-89-1SDS

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 (2S)-2-formamido-3-methyl-3-sulfanylbutanoic acid

1.2 Other means of identification

Product number -
Other names D-Valine,N-formyl-3-mercapto

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:13833-89-1 SDS

13833-89-1Relevant academic research and scientific papers

Preparation of Some Novel S-Nitroso Compounds as Potential Slow-release Agents of Nitric Oxide in vivo

Moynihan, Humphrey A.,Roberts, Stanley M.

, p. 797 - 806 (2007/10/02)

The optimum conditions for the preparation of N-acetyl-S-nitrosopenicillamine (SNAP) 3 were determined and applied to the synthesis of the corresponding N-formyl compound 7.The nitrosation of penicillamine dipeptides was investigated and bis-thionitroso compounds 13, 18, 26 and 27 were isolated.S,S'-Dinitroso dithiol 13 showed biological activity akin to that of glyceryl trinitrate in decreasing systemic arterial blood pressure in anaesthetized rats and rabbits.Concomitant inhibition of collagen- or ADP-induced platelet aggregation was observed.

Aqueous and Anhydrous Degradations of 6α-Formamidopenicillins

Cutmore, E. Alan,Guest, Angela W.,Hatto, Julia D. I.,Moores, Clive J.,Smale, Terence C.,et al.

, p. 847 - 853 (2007/10/02)

When an aqueous solution of the 6α-formamidopennicilin BRL 36650 (1) was set aside for 36 h, an essentially quantitative C(5)-C(6) cleavage resulted, yielding the α,α-bis(acylamino) acid (6) and N-formylpenicillamine (10).The unsubstituted phenyl compound

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