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(2S)-2-(acetylamino)-N-[(2S)-2-{[(1S)-3-chloro-1-methyl-2-oxopropyl]amino}propanoyl]propanamide is a complex organic compound with a non-preferred name, which can be simplified as a derivative of proline. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it contains a chlorine atom, which contributes to its unique properties. (2S)-2-(acetylamino)-N-[(2S)-2-{[(1S)-3-chloro-1-methyl-2-oxopropyl]amino}propanoyl]propanamide (non-preferred name) is characterized by its acetylamino group, a proline-based structure, and a 3-chloro-1-methyl-2-oxopropyl moiety. It is likely to be found in pharmaceutical or chemical research settings, where its specific stereochemistry and functional groups may be of interest for the development of new drugs or materials.

38320-48-8

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38320-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38320-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38320-48:
(7*3)+(6*8)+(5*3)+(4*2)+(3*0)+(2*4)+(1*8)=108
108 % 10 = 8
So 38320-48-8 is a valid CAS Registry Number.

38320-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ac-Ala2-AlaCH2Cl

1.2 Other means of identification

Product number -
Other names (S)-2-((S)-2-Acetylamino-propionylamino)-N-((S)-3-chloro-1-methyl-2-oxo-propyl)-propionamide

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:38320-48-8 SDS

38320-48-8Downstream Products

38320-48-8Relevant academic research and scientific papers

Thermitase - A Thermostable Serine Protease. II. Synthesis of Substrate Analogous Peptide Chloromethyl Ketones as Irreversibly Acting Inhibitors

Jahreis, Guenther,Smalla, Kornelia,Fittkau, Siegfried

, p. 41 - 47 (2007/10/02)

The preparation of dipeptide to pentapeptide chloromethyl ketones of alanine with variation of the amino acid in the P1 and P2 position of the peptides is described.The synthesis is performed by fragment condensation of N-acylated amino acids or peptides with the unprotected chloromethyl ketone derivatives of amino acids and peptides, respectively.Some examples of enzyme inactivation by peptide chloromethyl ketones are discussed.

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