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129540-21-2

129540-21-2

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129540-21-2 Usage

General Description

2-(2-Chlorophenyl)pyrrolidine is a chemical compound with the molecular formula C10H12ClN. It is a pyrrolidine derivative, which means it contains a five-membered ring structure with a heteroatom nitrogen. The compound has a 2-chlorophenyl group attached to the pyrrolidine ring. 2-(2-Chlorophenyl)pyrrolidine is used in organic synthesis and medicinal chemistry, and it may have various pharmacological activities, including potential use as a psychoactive drug. It is important to handle this chemical with caution and follow proper safety protocols due to the potential hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 129540-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,4 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129540-21:
(8*1)+(7*2)+(6*9)+(5*5)+(4*4)+(3*0)+(2*2)+(1*1)=122
122 % 10 = 2
So 129540-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12ClN/c11-9-5-2-1-4-8(9)10-6-3-7-12-10/h1-2,4-5,10,12H,3,6-7H2

129540-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Chlorophenyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names -

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:129540-21-2 SDS

129540-21-2Relevant articles and documents

Stereocomplementary Synthesis of Pharmaceutically Relevant Chiral 2-Aryl-Substituted Pyrrolidines Using Imine Reductases

Chen, Fei-Fei,Chen, Qi,Li, Bo-Bo,Xu, Jian-He,Zhang, Yu-Hui,Zheng, Gao-Wei,Zhou, Xin-Yi

supporting information, p. 3367 - 3372 (2020/04/21)

Exploring a collection of naturally occurring imine reductases (IREDs) identified two stereocomplementary IREDs with reducing activity toward sterically hindered 2-aryl-substituted pyrrolines. Using (R)-selective ScIR and (S)-selective SvIR, various chiral 2-aryl-substituted pyrrolidines with excellent enantioselectivity (>99% ee) were stereocomplementarily synthesized in good yield (60-80%), demonstrating the feasibility of IREDs for generating pharmaceutically relevant chiral 2-aryl-substituted pyrrolidine intermediates.

Pyrroloisoquinoline antidepressants. 3. A focus on serotonin

Maryanoff,Vaught,Shank,McComsey,Costanzo,Nortey

, p. 2793 - 2797 (2007/10/02)

A collection of hexahydropyrroloisoquinoline derivatives (1-22), which represent a class of compounds that inhibit the neuronal uptake of dopamine (DA), norepinephrine (NE), and serotonin (5-HT), was investigated in vivo for serotonin-potentiating propert

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