127073-80-7 Usage
Description
Pyrrolidine, 3-(1-methylethenyl)-1-(phenylmethyl)is a heterocyclic organic compound with a five-membered ring containing one nitrogen atom. It is primarily used in pharmaceuticals as a building block for the synthesis of various drugs.
Used in Pharmaceutical Industry:
Pyrrolidine, 3-(1-methylethenyl)-1-(phenylmethyl)is used as a building block for the synthesis of various medications for different medical conditions, such as antipsychotic and antiepileptic drugs, antibiotics, and antidepressants. Its structure and properties make it a valuable intermediate in the production of a wide range of pharmaceuticals, making it a crucial chemical in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 127073-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,7 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127073-80:
(8*1)+(7*2)+(6*7)+(5*0)+(4*7)+(3*3)+(2*8)+(1*0)=117
117 % 10 = 7
So 127073-80-7 is a valid CAS Registry Number.
127073-80-7Relevant articles and documents
Intramolecular carbolithiation reactions for the preparation of 3-alkenylpyrrolidines.
Coldham, Iain,Price, Kathy N,Rathmell, Richard E
, p. 2111 - 2119 (2007/10/03)
Tin-lithium exchange allows the formation of alpha-amino-organolithium species that undergo anionic cyclization onto allylic ethers to give 3-alkenylpyrrolidines. The methodology has been applied to the synthesis of an advanced intermediate related to the natural product (-)-alpha-kainic acid.
TiCL4 INDUCED IMINIUM ION CYCLIZATIONS OF α-CYANOAMINES
Yang, Teng-Kuei,Hung, Shun-Ming,Lee, Dong-Sheng,Hong, An-Way,Cheng, Chan-Chun
, p. 4973 - 4976 (2007/10/02)
Tertiary α-cyanoamines served as the precursors of iminium ions in the presence of titanium tetrachloride.Various intramolecular nucleophiles, olefinic and acetylenic, were found to produce cyclized products.The influences of ring sizes and substitutions on the double bonds were also investigated.
