383127-62-6 Usage
General Description
2-(4-Methylbenzyl)pyrrolidine, also known by its chemical formula C14H19N, is a compound belonging to the class of pyrrolidine derivatives. It is a colorless to pale yellow liquid with a molecular weight of 205.31 g/mol. This chemical is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical products. It is also utilized in the production of perfumes and flavorings due to its aromatic properties. Additionally, 2-(4-Methylbenzyl)pyrrolidine is employed as a reagent in organic synthesis and chemical research. Due to its potential toxicity and hazardous properties, proper safety precautions and handling procedures should be followed when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 383127-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,1,2 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 383127-62:
(8*3)+(7*8)+(6*3)+(5*1)+(4*2)+(3*7)+(2*6)+(1*2)=146
146 % 10 = 6
So 383127-62-6 is a valid CAS Registry Number.
383127-62-6Relevant articles and documents
CYCLIC AMINE COMPOUNDS
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Page/Page column 49; 54, (2011/10/19)
Problems to be solved are to provide novel low-molecular compounds which exhibit calcium receptor antagonist activity, and which are highly safe and orally administrable. As a means for solving the problems, compounds having the Formula (I) or pharmaceuti
Asymmetric synthesis of 5-arylmethylpyrrolidin-2-ones and 2-arylmethylpyrrolidines
Lebrun, Stephane,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre
, p. 2625 - 2632 (2007/10/03)
An efficient methodology for the enantioselective synthesis of 5-arylmethylpyrrolidin-2-ones and 2-arylmethylpyrrolidines has been devised. The key step is the stereoselective hydrogenation of the N-acylhydrazonium salts obtained from the corresponding arylmethylene hydrazides. These highly conjugated compounds are readily prepared by reacting a chiral succinimide with a variety of arylmethyl Grignard reagents. Removal of the chiral auxiliary and subsequent reduction complete the synthesis of the title compounds.
