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(2S)-2-[N'-(tert-Butoxycarbonyl)hydrazinocarbonyl]-1-pyrrolidinecarboxylic acid benzyl ester is a complex organic compound with the molecular formula C16H22N2O4. It is a chiral molecule, indicated by the "2S" notation, which specifies the configuration of the molecule's chiral center. The compound features a pyrrolidine ring, a benzyl ester group, and a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in peptide synthesis to protect amino groups. This specific chemical structure suggests potential applications in pharmaceuticals or as an intermediate in the synthesis of more complex molecules, given its protective and functional groups.

53157-64-5

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53157-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53157-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,5 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53157-64:
(7*5)+(6*3)+(5*1)+(4*5)+(3*7)+(2*6)+(1*4)=115
115 % 10 = 5
So 53157-64-5 is a valid CAS Registry Number.

53157-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-Pro-NHNHBoc

1.2 Other means of identification

Product number -
Other names (S)-2-(N'-tert-Butoxycarbonyl-hydrazinocarbonyl)-pyrrolidine-1-carboxylic acid benzyl ester

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:53157-64-5 SDS

53157-64-5Relevant academic research and scientific papers

Synthesis of an L-proline modified mimetic of the A83586C antitumour cyclodepsipeptide

Hale, Karl J.,Lazarides, Linos

, p. 1832 - 1833 (2007/10/03)

A mimetic of the A83586C cyclodepsipeptide has been synthesised via a three-segment coupling protocol involving dipeptides 9, 8 and 7; in contrast to our previous synthesis of A83586C, where the HATU-mediated macrolactamisation proceeded in 25% yield, the

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