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Butanamide, 2-amino-4-(methylsulfinyl)-, (S)-, also known as (S)-2-Amino-4-(methylsulfinyl)butanamide, is a chiral organic compound with the molecular formula C5H12N2O2S. It is a derivative of butanamide, featuring an amino group at the 2nd position and a methylsulfinyl group at the 4th position. The (S)- configuration indicates that the compound has a specific arrangement of atoms in its chiral center, which is crucial for its biological activity and potential applications. Butanamide, 2-amino-4-(methylsulfinyl)-, (S)- is of interest in the field of pharmaceuticals and organic chemistry, as its unique structure may confer specific properties that can be harnessed in the development of new drugs or chemical processes.

7536-72-3

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7536-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7536-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7536-72:
(6*7)+(5*5)+(4*3)+(3*6)+(2*7)+(1*2)=113
113 % 10 = 3
So 7536-72-3 is a valid CAS Registry Number.

7536-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-4-methylsulfinylbutanamide

1.2 Other means of identification

Product number -
Other names Butanamide,2-amino-4-(methylsulfinyl)-,(S)

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 -
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More Details:7536-72-3 SDS

7536-72-3Relevant academic research and scientific papers

α-Aminonitrile hydration in the presence of hydrogen peroxide in aqueous basic medium

Taillades, Jacques

, p. 89 - 100 (2007/10/03)

α-Aminonitriles are hydrated into α-aminoamides in the presence of hydrogen peroxide in sodic or ammoniacal basic medium. While the hydration mechanism is close to the mechanism described previously in the case of aromatic nitrites, we showed that, in weakly basic conditions, the amine function of α-aminonitrile is competitively oxidized via a peroxyimidic acid by an intramolecular process. In the case of 2-aminopropanenitrile, this reaction leads to pyruvamide oxime. Furthermore, the study of structurereactivity relationships in the hydration of aliphatic and aromatic monofunctional nitriles and α-aminonitriles showed that the reactivity of the substrates towards hydroperoxide onion, which mostly depends on inductive effects of the substituents, is sufficiently enhanced to allow hydration of tertiary α-aminonitriles with low steric hindrance and regioselective hydration of dissymmetric α-aminodinitriles. Eisevier,.

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