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H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH is a chiral peptide derivative of proline with a Boc protecting group and an ester functional group attached to the side chain of the proline residue. H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH exhibits asymmetric 2S,4R stereochemistry, which is crucial for its specific interactions and applications in various fields.

556796-29-3

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556796-29-3 Usage

Uses

Used in Organic Synthesis:
H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH is used as a chiral building block in organic synthesis for the preparation of complex organic molecules and pharmaceutical compounds. Its unique stereochemistry and functional groups enable selective reactions and the formation of desired products with high enantioselectivity and diastereoselectivity.
Used in Drug Development:
H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH is used as a key intermediate in the synthesis of bioactive peptides and peptidomimetics with potential therapeutic applications. H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH's specific stereochemistry and functional groups can be exploited to design and develop novel drugs with improved pharmacological properties, such as enhanced bioavailability, selectivity, and reduced side effects.
Used in Pharmaceutical Industry:
H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH is used as a chiral resolving agent in the synthesis of enantiomerically pure pharmaceutical compounds. Its unique stereochemistry allows for the efficient separation of enantiomers, ensuring the production of high-quality, single-enantiomer drugs with improved safety and efficacy profiles.
Used in Research and Development:
H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH is used as a research tool in the study of peptide chemistry, stereochemistry, and the development of novel synthetic methods. Its unique structural features provide valuable insights into the understanding of peptide conformation, folding, and interactions with biological targets, paving the way for the discovery of new therapeutic agents and synthetic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 556796-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,7,9 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 556796-29:
(8*5)+(7*5)+(6*6)+(5*7)+(4*9)+(3*6)+(2*2)+(1*9)=213
213 % 10 = 3
So 556796-29-3 is a valid CAS Registry Number.

556796-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name H-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH

1.2 Other means of identification

Product number -
Other names (2S,4R)-Pro(4-OCO-NH-CH2-CH2-NH-Boc)-OH

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:556796-29-3 SDS

556796-29-3Relevant academic research and scientific papers

A novel somatostatin mimic with broad somatotropin release inhibitory factor receptor binding and superior therapeutic potential

Lewis, Ian,Bauer, Wilfried,Albert, Rainer,Chandramouli, Nagarajan,Pless, Janos,Weckbecker, Gisbert,Bruns, Christian

, p. 2334 - 2344 (2003)

A rational drug design approach, capitalizing on structure-activity relationships and involving transposition of functional groups from somatotropin release inhibitory factor (SRIF) into a reduced size cyclohexapeptide template, has led to the discovery o

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