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122442-02-8

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122442-02-8 Usage

General Description

(S)-2-(pyrrolidin-3-yl)acetic acid is a chemical compound with the molecular formula C7H11NO2. It falls under the class of organic compounds known as pyrrolidines, which are compounds containing a pyrrolidine ring, a five-membered saturated ring with one nitrogen atom and four carbon atoms. The '(S)' prefix indicates a specific stereochemistry, which means the atoms in the molecule are arranged in a particular three-dimensional orientation. Due to the presence of the carboxylic acid and nitrogen groups in the compound, it is likely to have both acidic and basic properties. It could have potential applications in medicinal chemistry and drug discovery, as several pyrrolidine derivatives are known to have pharmacological activities. However, specific information on (S)-2-(pyrrolidin-3-yl)acetic acid’s properties and uses is relatively limited.

Check Digit Verification of cas no

The CAS Registry Mumber 122442-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,4 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122442-02:
(8*1)+(7*2)+(6*2)+(5*4)+(4*4)+(3*2)+(2*0)+(1*2)=78
78 % 10 = 8
So 122442-02-8 is a valid CAS Registry Number.

122442-02-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3S)-pyrrolidin-3-yl]acetic acid

1.2 Other means of identification

Product number -
Other names RW3881

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:122442-02-8 SDS

122442-02-8Downstream Products

122442-02-8Relevant articles and documents

Enantioselective Three-Step Synthesis of Homo-β-proline: A Donor-Acceptor Cyclopropane as Key Intermediate

Pilsl, Ludwig K. A.,Ertl, Thomas,Reiser, Oliver

, p. 2754 - 2757 (2017)

An enantioselective three-step synthesis of the GABA uptake inhibitor (S)-(+)-homo-β-proline was developed. The basis for the synthesis was the enantioselective CuI-catalyzed cyclopropanation of N-Boc-pyrrole, a substrate that persistently has proved to be challenging in such transformations. The cyclopropanation can be performed on a 150 mmol scale, and the two subsequent steps (i.e., hydrogenation and in situ cyclopropane-opening/double-deprotection) toward the target molecule proceed smoothly in quantitative yield without loss of enantiopurity.

Chiral bicyclic guanidine as a versatile bronsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters

Ye, Weiping,Jiang, Zhiyong,Zhao, Yujun,Goh, Serena Li Min,Leow, Dasheng,Soh, Ying-Teck,Tan, Choon-Hong

, p. 2454 - 2458 (2008/09/19)

A chiral bicyclic guanidine was developed as a versatile Bronsted base catalyst for the enantioselective Michael reactions of dithiomalonates and β-keto thioesters using a range of acceptors including maleimides, cyclic enones, furanone and acyclic 1,4-di

Conformationally constrained no synthase inhibitors: Rigid analogs of L- N-iminoethylornithine

Eustache, Jacques,Grob, Alfred,Lam, Charles,Sellier, Odile,Schulz, Gerhard

, p. 2961 - 2966 (2007/10/03)

The synthesis of eight rigid analogs of L-N-iminoethylomithine (L-NIO) is described. The compounds have been evaluated for their inhibition of inducible nitric oxide synthase. Preliminary structure-activity relationships are discussed.

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