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.
1189152-82-6Relevant 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.