71424-66-3 Usage
Structure
Cyclopropa-cyclohepta-indene with a hydroxyl group, a methyl group, and a methylene group
Rings
Cyclopropyl and cycloheptadiene
Stereocenters
Eight (1,1a,4,5,7,8,9,9a)
Chirality
Highly chiral due to the presence of eight stereocenters
Stereodescriptors
β and α symbols denote the stereochemistry at the stereocenters
Functional Groups
Hydroxyl (-OH), Methyl (-CH3), and Methylene (-CH2-)
Potential Applications
Organic synthesis, pharmaceuticals, materials science
Molecular Architecture
Unique and intricate due to the presence of multiple rings, stereocenters, and functional groups
Check Digit Verification of cas no
The CAS Registry Mumber 71424-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,2 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71424-66:
(7*7)+(6*1)+(5*4)+(4*2)+(3*4)+(2*6)+(1*6)=113
113 % 10 = 3
So 71424-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O2/c1-9-6-7-13-17(20(13,4)5)15-11(3)19(22)12-8-10(2)18(21)16(12)14(9)15/h10,13,17,22H,1,6-8H2,2-5H3/t10-,13?,17?/m0/s1
71424-66-3Relevant academic research and scientific papers
Total Synthesis of (+)-Jatropholone A and B
Smith, Amos B.,Liverton, Nigel J.,Hrib, Nicholas J.,Sivaramakrishnan, Hariharan,Winzenberg, Kevin
, p. 3239 - 3241 (2007/10/02)
The first total synthesis of jatropholones A and B in homochiral form is disclosed; the absolute stereochemistry is thereby established.
