420802-63-7 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4,7b,8,9,10,10a-octahydro-1H-cyclopenta[b][1,4]diazepino[6,7,1-hi]indole is used as a potential pharmaceutical candidate for [application reason] due to its structural similarity to natural products and known bioactive compounds. Its heterocyclic nature and the presence of a diazepine ring fused to a cyclopentane and indole ring may contribute to its potential applications in medicinal chemistry and drug discovery.
(Note: The specific application reason is not provided in the materials, so it is left as "[application reason]". Further research is needed to determine the exact uses and potential biological activities of 2,3,4,7b,8,9,10,10a-octahydro-1H-cyclopenta[b][1,4]diazepino[6,7,1-hi]indole in the pharmaceutical industry.)
Check Digit Verification of cas no
The CAS Registry Mumber 420802-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,0,8,0 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 420802-63:
(8*4)+(7*2)+(6*0)+(5*8)+(4*0)+(3*2)+(2*6)+(1*3)=107
107 % 10 = 7
So 420802-63-7 is a valid CAS Registry Number.
420802-63-7Relevant academic research and scientific papers
A process for the preparation of 1,2,3,4,8,9,10,10a-octahydro-7bH- cyclopenta[b][1,4]diazepino[6,7,1-hi]indole
Welmaker, Gregory S.,Sabalski, Joan E.
, p. 4851 - 4854 (2007/10/03)
A synthesis of 1,2,3,4,8,9,10,10a-octahydro-7bH-cyclopenta[b][1,4] diazepino[6,7,1-hi]indole is described exemplifying a new synthetic route to medicinally interesting compounds. The key step involves a cyclization of 2-(2,3,3a,8b-tetrahydrocyclopenta[b]indol-4(1H)-yl)-ethanamine with aqueous formaldehyde in the presence of trifluoroacetic acid.
