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(2R,4S)-4-(aMinoMethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid, also known as Boc-D-Pro-NH2, is a chemical compound that features an amino group (NH2) and a pyrrolidine ring. It is widely utilized in peptide chemistry as a fundamental building block for the assembly of larger peptides and proteins. The presence of the tert-butoxycarbonyl (Boc) group serves as a protective group for the amino group, enabling selective reactions at other functional groups without interference from the amino group. (2R,4S)-4-(aMinoMethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid holds significant value in medicinal chemistry and drug development due to its potential use in the synthesis of new therapeutic agents.

132622-86-7

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132622-86-7 Usage

Uses

Used in Pharmaceutical Industry:
(2R,4S)-4-(aMinoMethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is used as a building block for the synthesis of peptides and proteins, which are vital for developing new drugs and therapies. Its role in creating complex peptide structures allows researchers to explore a wide range of applications, from treating various diseases to enhancing drug delivery systems.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (2R,4S)-4-(aMinoMethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is employed as a key component in the development of novel compounds with potential therapeutic applications. Its unique structure and the protective Boc group enable the design and synthesis of innovative pharmaceutical agents that can address unmet medical needs.
Used in Peptide Synthesis:
(2R,4S)-4-(aMinoMethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is used as a starting material in the synthesis of various peptides. Its presence in peptide chains can contribute to the overall function and stability of the peptide, making it an essential component in the creation of bioactive molecules for research and therapeutic purposes.
Used in Drug Development:
As a compound with potential therapeutic applications, (2R,4S)-4-(aMinoMethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is utilized in drug development to create new pharmaceuticals. Its ability to be incorporated into larger peptide structures allows for the exploration of its potential in treating a variety of medical conditions, making it a valuable asset in the development of innovative treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 132622-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132622-86:
(8*1)+(7*3)+(6*2)+(5*6)+(4*2)+(3*2)+(2*8)+(1*6)=107
107 % 10 = 7
So 132622-86-7 is a valid CAS Registry Number.

132622-86-7SDS

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 (4R)-1-(tert-butoxycarbonyl)-4-(aminomethyl)-D-proline

1.2 Other means of identification

Product number -
Other names (2R,4S)-4-Aminomethyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl 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:132622-86-7 SDS

132622-86-7Relevant academic research and scientific papers

Conformationally Restricted Arginine Analogues

Webb, Thomas R.,Eigenbrot, Charles

, p. 3009 - 3016 (2007/10/02)

We report the practical synthesis and structural characterization of a set of conformationally constrained protected arginine analogues.These enantiomerically pure analogues have the general structure 1 and are prepared in seven to eight steps from the co

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