100414-86-6 Usage
General Description
[(1R,2R)-2-(1H-Indol-2-yl)-2-methyl-cyclohexyl]-methanol is a chemical compound with a complex structure. It contains a cyclohexane ring with a methyl group attached to a carbon atom, as well as an indole ring fused to the cyclohexane ring. The compound also contains a hydroxyl group, which is attached to the cyclohexane ring. This chemical is a derivative of cyclohexane and indole, and it is a chiral compound, meaning it has two stereoisomeric forms. This chemical may have potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications.
Check Digit Verification of cas no
The CAS Registry Mumber 100414-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,1 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100414-86:
(8*1)+(7*0)+(6*0)+(5*4)+(4*1)+(3*4)+(2*8)+(1*6)=66
66 % 10 = 6
So 100414-86-6 is a valid CAS Registry Number.
100414-86-6Relevant articles and documents
ORGANOMETALLIC REAGENTS IN SYNTHESIS A NEW PROTOCOL FOR CONSTRUCTION OF THE INDOLE NUCLEUS
Smith, III, Amos B.,Visnick, Melean,Haseltine, John N.,Sprengeler, Paul A.
, p. 2957 - 2970 (2007/10/02)
Organodilithium reagents derived from 2-alkyl-N-trimethylsilyl anilines undergo condensation with esters of carboxylic acids to afford substituted indoles.A total of 16 examples are reported; yields in general were good.In conjuction with this program, a convenient, large-scale procedure for preparation of monosilylated anilines was also developed.To demonstrate the utility of the new indole protocol in natural products synthesis, efficient syntheses of (+)-cinchonamine and (+)-epi-cinchonamine as well as a tetracyclic model system for the architecturally complex penitrem mycotoxins were completed in regio- and stereoselective fashion.
