155503-32-5 Usage
General Description
"(2-CHLORO-BENZYL)-[2-(1 H-INDOL-3-YL)-ETHYL]-AMINE" is a chemical compound with a molecular formula C17H18CIN2. It is a derivative of benzylamine and contains a chlorine atom attached to a benzene ring. It also contains an indole group, which is a bicyclic compound commonly found in many natural products and pharmaceuticals. The compound is a tertiary amine, meaning it contains three alkyl or aryl groups attached to the nitrogen atom. "(2-CHLORO-BENZYL)-[2-(1 H-INDOL-3-YL)-ETHYL]-AMINE" may have potential applications in the pharmaceutical industry, particularly in the development of new drugs with indole or amine moieties.
Check Digit Verification of cas no
The CAS Registry Mumber 155503-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 155503-32:
(8*1)+(7*5)+(6*5)+(5*5)+(4*0)+(3*3)+(2*3)+(1*2)=115
115 % 10 = 5
So 155503-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H17ClN2/c18-16-7-3-1-5-14(16)11-19-10-9-13-12-20-17-8-4-2-6-15(13)17/h1-8,12,19-20H,9-11H2/p+1
155503-32-5Relevant articles and documents
Indole derivatives with antimycobacterial activity
Mahboobi,Grothus,Meindl
, p. 105 - 114 (2007/10/02)
1,3-Dinitro-2-(indol-3'-yl)-propanes 3 are synthesized by Michael reaction of nitromethane with the indolylnitroethenes 2. - Reaction of the aldehydes 4 and 10 with the benzylamines 12 as well as the reaction of the indolylalkylamines 6a and 9a with the benzaldehydes 11 lead to Schiff bases which are reduced to N-benzyl-(indol-3-ylmethyl)-amines 13 and N-benzyl-(indol-3-ylethyl)-amines 14, respectively; tert amines 16 are synthesized via the formamides 15, amines 18 are prepared according to Mannich. - Inhibitory effects on Mycobacterium tuberculosis H 37 Ra are investigated, a structure-activity relationship is discussed.
