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1-[(Benzyloxy)carbonyl]pyrrolidine-2-carboxylic acid is a chemical compound characterized by the molecular formula C16H19NO5. It is a white to off-white solid that serves as a crucial protecting group for amino acids in organic synthesis. 1-[(BENZYLOXY)CARBONYL]PYRROLIDINE-2-CARBOXYLIC ACID features a pyrrolidine ring with a carboxylic acid and a benzyloxy carbonyl group attached, providing stability under normal conditions and making it a valuable reagent in organic chemistry for a variety of applications.

5618-96-2

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5618-96-2 Usage

Uses

Used in Organic Synthesis:
1-[(Benzyloxy)carbonyl]pyrrolidine-2-carboxylic acid is used as a protecting group for amino acids in organic synthesis to prevent unwanted reactions from occurring at the amino group. This protection is essential for the successful synthesis of peptide and protein molecules, ensuring the correct formation of peptide bonds and maintaining the integrity of the final product.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-[(Benzyloxy)carbonyl]pyrrolidine-2-carboxylic acid is used as a key intermediate in the synthesis of various drug molecules. Its ability to protect amino groups allows for the controlled formation of complex peptide-based drugs, facilitating the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Research and Development:
1-[(Benzyloxy)carbonyl]pyrrolidine-2-carboxylic acid is utilized in research and development for the study of peptide and protein chemistry. It aids in understanding the fundamental principles of peptide bond formation and the role of protecting groups in the synthesis of bioactive peptides and proteins.
Used in Biochemistry and Molecular Biology:
In the fields of biochemistry and molecular biology, 1-[(Benzyloxy)carbonyl]pyrrolidine-2-carboxylic acid is employed as a tool for the synthesis and modification of peptides and proteins. Its use in protecting amino groups allows researchers to explore the structure-function relationships of these biomolecules and develop a deeper understanding of their biological roles and potential applications in medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 5618-96-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5618-96:
(6*5)+(5*6)+(4*1)+(3*8)+(2*9)+(1*6)=112
112 % 10 = 2
So 5618-96-2 is a valid CAS Registry Number.

5618-96-2SDS

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 N-Cbz-DL-proline

1.2 Other means of identification

Product number -
Other names 1-((benzyloxy)carbonyl)pyrrolidine-2-carboxylic acid

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:5618-96-2 SDS

5618-96-2Relevant academic research and scientific papers

3-ACYL- AND 3-ALKOXYCARBONYL-2-OXAZOLONES AND THEIR HOMOPOLYMERS AS AMINO-PROTECTING REAGENTS

Kunieda, Takehisa,Higuchi, Tsunehiko,Abe, Yoshihiro,Hirobe, Masaaki

, p. 3065 - 3066 (2007/10/02)

3-Acyl and 3-alkoxycarbonyl-2-oxazolones as well as their homopolymers serve as practically usefull N-protecting reagents of amines including α-amino acids.

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