84218-37-1 Usage
Core structure
The chemical has a core structure of isoquinoline, which is a bicyclic aromatic compound with one nitrogen atom in the ring.
Substitution
The isoquinoline ring is substituted with a methanamine group (-NH-CH3) and a 3,4-dihydro ring.
Halogenation
One of the phenyl rings is substituted with a chlorine atom (-Cl).
Methoxylation
Both the phenyl and isoquinoline rings are methoxylated (-O-CH3).
Indole group
The chemical contains an indole group, which is a bicyclic aromatic compound with a nitrogen atom in one of the rings.
Psychoactive substance
The chemical is a psychoactive substance that acts as a serotonin receptor agonist and has hallucinogenic effects.
Danger
The compound can be dangerous and has been associated with adverse health effects.
Check Digit Verification of cas no
The CAS Registry Mumber 84218-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,1 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84218-37:
(7*8)+(6*4)+(5*2)+(4*1)+(3*8)+(2*3)+(1*7)=131
131 % 10 = 1
So 84218-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H28ClN3O2/c1-32-26-14-18-11-12-31(17-30-24-10-6-4-8-22(24)28)25(21(18)15-27(26)33-2)13-19-16-29-23-9-5-3-7-20(19)23/h3-10,14-16,25,29-30H,11-13,17H2,1-2H3
84218-37-1Relevant articles and documents
Antiinflammatory and antiproteolytic activities of newer indolyl isoquinolines
Tandon,Tandon,Barthwal,Bhalla,Bhargava
, p. 1233 - 1235 (2007/10/02)
Several indolyl isoquinoline derivatives were synthesized and evaluated for their antiinflammatory and antiproteolytic activities. These derivatives possessed 9.2-32.4% inhibition at a dose of 100 mg/kg i.p. against carrageenin-induced oedema. Four of the
