104672-02-8 Usage
General Description
(S)-butyl indoline-2-carboxylate, also known as (S)-2-carboxybutylindoline, is a chemical compound belonging to the class of indoline derivatives. It is a chiral molecule with a butyl side chain attached to the indoline ring. (S)-butyl indoline-2-carboxylate is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its ability to serve as a versatile building block in organic chemistry. It has also been investigated for its potential biological and pharmacological properties, showing promise as a potential drug candidate. Overall, (S)-butyl indoline-2-carboxylate is a valuable chemical with a wide range of applications in the field of organic synthesis and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 104672-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,7 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104672-02:
(8*1)+(7*0)+(6*4)+(5*6)+(4*7)+(3*2)+(2*0)+(1*2)=98
98 % 10 = 8
So 104672-02-8 is a valid CAS Registry Number.
104672-02-8Relevant articles and documents
Stereoselective synthesis of optically active cyclic α- And β-amino esters through lipase-catalyzed transesterification or interesterification processes
Alatorre-Santamaria, Sergio,Gotor-Fernandez, Vicente,Gotor, Vicente
experimental part, p. 2307 - 2313 (2010/11/05)
A series of cyclic α- and β-amino esters belonging to a family of indolines and quinolines have been efficiently synthesized to study their behavior in lipase-mediated kinetic resolution reactions. The influence of the fused ring structure to the benzene ring and the position of the ester functionality relative to the amino group have been demonstrated, finding excellent values of enantiodiscrimination in the transesterification reaction of methyl indoline-3-carboxylate with n-butanol catalyzed by Candida antarctica lipase B being observed. On the other hand, low to moderate selectivities have been found when using a wide panel of lipases toward methyl indoline-2- carboxylate or 1,2,3,4-tetrahydroquinoline derivatives in alkoxycarbonylation, transesterification or interesterification reactions.
