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1189152-82-6

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1189152-82-6 Usage

General Description

"(S)-2-(4-Bromophenyl)pyrrolidine" is a chemical compound with a molecular formula C10H12BrN. It is a member of the pyrrolidine class of compounds, which are cyclic amines. The compound contains a four-membered ring structure with a pyrrolidine group attached to a 4-bromophenyl group. (S)-2-(4-BROMOPHENYL)PYRROLIDINE has potential applications in various fields such as pharmaceuticals, agrochemicals, and materials science. The 4-bromophenyl group imparts unique properties to the molecule and can potentially be used to synthesize various derivatives with different properties and functions. Additionally, the stereochemistry of the compound, denoted as (S), indicates the arrangement of atoms in space, which may influence its biological and chemical properties. Overall, "(S)-2-(4-Bromophenyl)pyrrolidine" is a versatile chemical compound with potential uses in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1189152-82-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,9,1,5 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1189152-82:
(9*1)+(8*1)+(7*8)+(6*9)+(5*1)+(4*5)+(3*2)+(2*8)+(1*2)=176
176 % 10 = 6
So 1189152-82-6 is a valid CAS Registry Number.

1189152-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(4-Bromophenyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names (S)-2-(4-bromophenyl)-pyrrolidine

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:1189152-82-6 SDS

1189152-82-6Downstream Products

1189152-82-6Relevant articles and documents

PROCESS FOR SYNTHESIS OF 2-SUBSTITUTED PYRROLIDINES AND PIPERADINES

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Page/Page column 61, (2011/09/19)

The present invention provides a highly efficient, versatile one-step process for asymmetric synthesis of either diastereomer of 2-substituted pyrrolidines from a single starting material with excellent yields and high diastereoselectivety. Also provided is a method for the asymmetric synthesis of both diastereomers of 2-substituted piperidines with good yields and excellent diastereoselectivety. Diasteroselectivity is controlled effectively by choice of reducing agent.

Asymmetric synthesis of 2-substituted pyrrolidines by addition of Grignard reagents to γ-chlorinated N-tert-butanesulfinyl imine

Reddy, Leleti Rajender,Prashad, Mahavir

supporting information; experimental part, p. 222 - 224 (2010/05/01)

A highly diastereoselective addition of various Grignard reagents to chiral γ-chlorinated N-tert-butanesulfinyl imine resulting in the formation of 2-substituted pyrrolidines is reported. This method is general and also efficient for the preparation of both enantiomers of 2-aryl, 2-alkyl and 2-vinyl substituted pyrrolidines in high yields.

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