30216-37-6 Usage
Chemical structure
A benzothiazole ring with a chlorinated phenyl group attached to an ethenyl group.
+ Potent and selective serotonin receptor agonist
mCPBG selectively binds to and activates serotonin receptors, particularly the 5-HT2A and 5-HT2C receptors.
+ Hallucinogenic
mCPBG can induce alterations in sensory perception and cognitive function, similar to effects produced by classic hallucinogens.
+ Synthetic compound
mCPBG is a man-made chemical and not found naturally in the environment.
+ Used in scientific research
mCPBG has been used to study the effects of serotonin on the brain and to investigate its potential therapeutic applications.
+ Controlled substance
Due to its psychoactive effects, mCPBG is classified as a controlled substance and is not approved for medical use.
+ Potential therapeutic applications
mCPBG has been investigated for its potential use in the treatment of various psychiatric disorders, but its use is limited due to its psychoactive properties.
Check Digit Verification of cas no
The CAS Registry Mumber 30216-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,1 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30216-37:
(7*3)+(6*0)+(5*2)+(4*1)+(3*6)+(2*3)+(1*7)=66
66 % 10 = 6
So 30216-37-6 is a valid CAS Registry Number.
30216-37-6Relevant academic research and scientific papers
Solid phase combinatorial synthesis of benzothiazoles and evaluation of topoisomerase II inhibitory activity
Choi, Suk-June,Park, Hyen Joo,Lee, Sang Kook,Kim, Sang Woong,Han, Gyoonhee,Choo, Hea-Young Park
, p. 1229 - 1235 (2007/10/03)
To investigate one possible mechanism of action of the cytotoxic activity of benzothiazoles, we synthesized 2-(substituted-phenyl)benzothiazoles and evaluated their ability to inhibit topoisomerase II activities. Solid phase combinatorial method using tri
Application of Phase-Transfer Catalysis to the Synthesis of Mono- and Bis-stilbenes and Styryls
Lokhande, S. B.,Rangnekar, D. W.
, p. 485 - 488 (2007/10/02)
A novel and convenient method has been developed for the synthesis of substituted stilbenes by the condensation of active methyl group in suitably substituted toluenes with aromatic aldehydes in aq. medium at room temperature using benzyltriethylammonium chloride as a phase-transfer catalyst.This method has also been applied for the preparation of heterocyclic styryls and extended to the synthesis of bis-stilbenes and bis-styryls using aromatic dialdehydes in place of monoaldehydes.A comparison of the results shows that the present method is superior to the conventional methods in many respects.
