114373-05-6 Usage
General Description
1-Benzyl-3-Methyl-Pyrrolidine-3-Carbonitrile is a chemical compound with the molecular formula C14H16N2. This organic compound is categorized under the class of pyrrolidines, which are compounds containing a pyrrolidine ring, a five-membered saturated heterocycle made up of four carbon atoms and a nitrogen atom. Its specific properties, such as its physical and chemical characteristics, toxicology, or potency, can vary and often need to be evaluated in a lab setting. It has potential utility in scientific research and development, particularly in the field of synthetic chemistry. However, it doesn't seem to be widely studied or used, and therefore, extensive data on its usage and effects may not be readily available.
Check Digit Verification of cas no
The CAS Registry Mumber 114373-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,7 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114373-05:
(8*1)+(7*1)+(6*4)+(5*3)+(4*7)+(3*3)+(2*0)+(1*5)=96
96 % 10 = 6
So 114373-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2/c1-13(10-14)7-8-15(11-13)9-12-5-3-2-4-6-12/h2-6H,7-9,11H2,1H3
114373-05-6Relevant articles and documents
[3+2] Dipolar cycloadditions of an unstabilised azomethine ylide under continuous flow conditions
Grafton, Mark,Mansfield, Andrew C.,Fray, M. Jonathan
scheme or table, p. 1026 - 1029 (2010/04/02)
The [3+2] dipolar cycloaddition reactions of the unstabilised azomethine ylide precursor benzyl(methoxymethyl)(trimethylsilylmethyl)amine with 12 electron-deficient alkenes in the presence of catalytic trifluoroacetic acid are examined under continuous fl
7-[[3-(aminomethyl)-3-alkyl]-1-pyrrolidinyl]-quinoline-carboxylic acids
-
, (2008/06/13)
Novel, orally active antibacterial agents are described and characterized as 7-[[3-(aminomethyl)-3-alkyl]-1-pyrrolidinyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acids or corresponding 1,8-naphthyridine derivatives as well as methods for their m
