121963-51-7 Usage
Structure
Contains a sulfonyl group and an indole ring
Member of
Indole family of organic compounds
Usage
Commonly used as a building block in organic synthesis
Potential applications
Development of pharmaceuticals, agrochemicals, and other fine chemicals
Known for
Use in research and development, particularly in the synthesis of new and complex organic molecules
Importance
Potential biological activities and therapeutic applications
Versatility
Valuable and versatile compound in the field of organic chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 121963-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,6 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121963-51:
(8*1)+(7*2)+(6*1)+(5*9)+(4*6)+(3*3)+(2*5)+(1*1)=117
117 % 10 = 7
So 121963-51-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO3S/c1-2-17(19)16-12-13-8-6-7-11-15(13)18(16)22(20,21)14-9-4-3-5-10-14/h3-12H,2H2,1H3
121963-51-7Relevant articles and documents
Synthesis of Alkyl-Substituted N-Protected Indoles via Acylation and Reductive Deoxygenation
Ketcha, Daniel M.,Lieurance, Brett A.,Homan, Dominic F. J.,Gribble, Gordin W.
, p. 4350 - 4356 (2007/10/02)
The synthesis of 2-, 3-, and 5-alkyl-1-(phenylsulfonyl)indoles involving Friedel-Crafts acylation followed by reductive deoxygenation is described.The application of this acylation-deoxygenation sequence to 3-acyl-1-(phenylsulfonyl)indoles bearing potenti
