18184-51-5 Usage
Molecular structure
1-hydroxy-3-methyl-2-(piperidin-1-ylmethyl)-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one is a chemical compound with a complex structure that includes a benzochromene core, a hydroxy group, a methyl group, and a piperidine moiety.
Derivative of THC
This compound is a derivative of tetrahydrocannabinol (THC), which is the psychoactive component of cannabis.
Contains a piperidine moiety
The presence of a piperidine group in the structure of this compound may contribute to its potential therapeutic properties.
Potential therapeutic properties
1-hydroxy-3-methyl-2-(piperidin-1-ylmethyl)-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one has been studied for its potential anti-inflammatory and analgesic effects.
Potential treatment for conditions
This compound has shown promise as a potential treatment for conditions such as chronic pain, neuropathic pain, and inflammation.
Potential as an anticancer agent
Further research is needed to determine the potential of this compound as an anticancer agent.
Ability to modulate the endocannabinoid system
This compound has been investigated for its potential to modulate the endocannabinoid system, which plays a role in various physiological processes.
Development of novel medications
Further research into the pharmacological properties of 1-hydroxy-3-methyl-2-(piperidin-1-ylmethyl)-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one could lead to the development of new medications for a variety of medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 18184-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,8 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18184-51:
(7*1)+(6*8)+(5*1)+(4*8)+(3*4)+(2*5)+(1*1)=115
115 % 10 = 5
So 18184-51-5 is a valid CAS Registry Number.
18184-51-5Relevant articles and documents
Modified coumarins. 7. Synthesis and biological activity of mannich bases of substituted 7,8,9,10-tetrahydrobenzo[c]chromen-6-ones
Garazd,Panteleimonova,Garazd,Khilya
, p. 532 - 538 (2002)
Condensation of 1- and 3-hydroxy-7,8,9,10-tetrahydrobenzo[c]chromen-6-ones with substituted 1,1-diaminomethanes produced Mannich bases containing a dialkylaminomethyl group in the 2- and 4-positions of 7, 8,9,10-tetrahydrobenzo[c]chromen-6-one. Pharmacological screening of 2-chloro-3-hydroxy-4-(1-pyrrolidinylmethyl)-7,8,9,10-tetrahydro-6H-benzo[c] chromen-6-one in Wistar rats showed that it possesses low toxicity and acts as a stimulant of the central and peripheral nervous systems with indications of neuroleptic and tranquilizing activities.
