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(2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is a complex chemical compound characterized by a pyrrolidine ring with an aminomethyl and a carboxylic acid functional group. The presence of the tert-butoxycarbonyl (Boc) group serves as a protecting agent for the amine functionality, which is crucial in organic synthesis. (2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid's stereochemistry, denoted by the (2S,4R) notation, specifies the arrangement of substituents around the chiral centers, contributing to its unique properties. (2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid holds potential for applications in various fields, including organic synthesis and pharmaceuticals, due to its distinctive structural features and functional groups.

132622-72-1

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132622-72-1 Usage

Uses

Used in Organic Synthesis:
(2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is used as an intermediate in organic synthesis for its ability to participate in a variety of chemical reactions due to its functional groups. The Boc-protected amine allows for selective reactions to occur at other sites within the molecule, which is crucial for the synthesis of complex organic compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is used as a building block for the development of new drugs. Its unique stereochemistry and functional groups can be leveraged to create molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Chiral Compound Synthesis:
(2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is utilized in the synthesis of chiral compounds, which are essential in many biological processes and have distinct pharmacological properties. The defined stereochemistry of (2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid makes it a valuable precursor for the production of enantiomerically pure substances.
Used in Chemical Research:
In the field of chemical research, (2S,4R)-4-(Aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid serves as a model compound for studying the effects of stereochemistry on chemical reactivity and biological activity. Understanding these effects can provide insights into the design of more effective and selective drugs and other chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 132622-72-1 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, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132622-72:
(8*1)+(7*3)+(6*2)+(5*6)+(4*2)+(3*2)+(2*7)+(1*2)=101
101 % 10 = 1
So 132622-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H20N2O4/c1-11(2,3)17-10(16)13-6-7(5-12)4-8(13)9(14)15/h7-8H,4-6,12H2,1-3H3,(H,14,15)/t7-,8+/m1/s1

132622-72-1SDS

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 (2S,4R)-4-(aminomethyl)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names D-mannitol 1,2:5,6-diacetonide 2,3-cyclic sulfate

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:132622-72-1 SDS

132622-72-1Relevant 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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