100234-62-6 Usage
General Description
1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol is a chemical compound with a complex and unique structure. It consists of an ethyl group, a methoxy group, and an indol-8-ol moiety. The presence of these groups gives it both aromatic and alcoholic properties. 1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indol-8-ol is a derivative of indole, a common organic compound found in many naturally occurring alkaloids. It is often used in research and pharmaceutical applications due to its potential biological activity and ability to interact with various receptors and enzymes in the body. Its exact functions and uses depend on its specific properties and the context in which it is utilized.
Check Digit Verification of cas no
The CAS Registry Mumber 100234-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,3 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100234-62:
(8*1)+(7*0)+(6*0)+(5*2)+(4*3)+(3*4)+(2*6)+(1*2)=56
56 % 10 = 6
So 100234-62-6 is a valid CAS Registry Number.
100234-62-6Relevant articles and documents
Synthetic studies on indoles and related compounds. Part 46.1 First total syntheses of 4, 8-dioxygenated β-carboline alkaloids
Suzuki, Hideharu,Unemoto, Minoru,Hagiwara, Mayumi,Ohyama, Takako,Yokoyama, Yuusaku,Murakami, Yasuoki
, p. 1717 - 1723 (2007/10/03)
Total syntheses of naturally occurring 4, 8-dioxygenated β-carboline alkaloids 2a, 2d, 2g, and 2h are described. The synthetic route involves two methodologies that we developed; (i) an improved Fischer indolization for the synthesis of a 7-oxygenated indole using a tosyl group for protection of the phenolic group, (ii) construction of a 4-methoxy-β-carboline skeleton by the C-3-selective cyclization of the C-2-substituent of the indole nucleus. The phenolic O-tosyl group of the β-carboline skeleton was successfully cleaved to the phenol by Na-anthracenide, and this phenol was methylated with TMSCH2N2.
