459868-73-6 Usage
Uses
Used in Pharmaceutical Research:
(R)-5-(2-aminopropyl)-1-(3-benzyloxypropyl) indoline-7-carbonitrile is used as a research compound for exploring its potential biological activities and interactions with biological targets. Its unique structure may offer insights into the development of new therapeutic agents.
Used in Drug Development:
In the pharmaceutical industry, (R)-5-(2-aminopropyl)-1-(3-benzyloxypropyl) indoline-7-carbonitrile is utilized as a lead compound in the discovery and optimization of new drugs. Its chiral property and functional groups may contribute to its selectivity and potency in modulating specific biological pathways.
Used in Chemical Synthesis:
(R)-5-(2-aminopropyl)-1-(3-benzyloxypropyl) indoline-7-carbonitrile serves as a key intermediate in the synthesis of more complex molecules with potential applications in various fields, including materials science and medicinal chemistry.
Used in Chiral Chemistry:
Due to its chiral nature, (R)-5-(2-aminopropyl)-1-(3-benzyloxypropyl) indoline-7-carbonitrile is employed in studies related to stereochemistry, enantioselective synthesis, and the investigation of the impact of stereoisomers on biological activity and pharmacokinetics.
Check Digit Verification of cas no
The CAS Registry Mumber 459868-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,8,6 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 459868-73:
(8*4)+(7*5)+(6*9)+(5*8)+(4*6)+(3*8)+(2*7)+(1*3)=226
226 % 10 = 6
So 459868-73-6 is a valid CAS Registry Number.
459868-73-6Relevant academic research and scientific papers
First asymmetric synthesis of Silodosin through catalytic hydrogenation by using Ir-SIPHOX catalysts
Yan, Pu-Cha,Zhang, Xian-Yi,Hu, Xiao-Wei,Zhang, Bin,Zhang, Xiang-Dong,Zhao, Michael,Che, Da-Qing,Li, Yuan-Qiang,Zhou, Qi-Lin
, p. 1449 - 1451 (2013/04/10)
An asymmetric synthesis of Silodosin was accomplished in high yield via catalytic hydrogenation of α,β-unsaturated carboxylic acid derivatives by using chiral catalyst Ir-SIPHOX, followed by Curtius rearrangement. Copyright
