58112-93-9

Usage

Type

Synthetic cannabinoid

Receptor

Acts as a potent agonist of the CB1 receptor

Family

Derivative of the indazole-3-carboxamide family

Pharmacological effects

Exhibits similar effects to other synthetic cannabinoids, including psychoactive and hallucinogenic properties

Adverse effects

Associated with severe toxicity, agitation, psychosis, and multiple fatalities

Legal status

Schedule I controlled substance in the United States and regulated in several countries due to potential for abuse and harm.

InChI:InChI=1/C16H14N2O/c1-18-14-10-6-5-9-13(14)17-16(18)11-15(19)12-7-3-2-4-8-12/h2-10H,11H2,1H3

Upstream product

• 13636-88-9 3,3-bis(methylthio)-1-phenylprop-2-en-1-one 
• 4760-34-3 N-methyl-1,2-phenylenediamine 
• 2876-08-6 1,2-dimethyl-1H-benzimidazole 
• 98-88-4 benzoyl chloride 
• 93-89-0 benzoic acid ethyl ester 

Downstream Products

• 103032-33-3 2-(4-diethylamino-phenylimino)-2-(1-methyl-1H-benzimidazol-2-yl)-1-phenyl-ethanone 
• 1026782-74-0 C₂₃H₁₇N₅O₂ 
• 1026769-34-5 C₂₆H₂₄N₄O₃ 
• 1025013-84-6 C₂₃H₁₈N₄ 
• 794582-42-6 C₂₃H₂₀N₄O 
• 1031872-85-1 C₂₄H₂₀N₄O 
• 1025014-25-8 C₂₂H₁₇N₅ 
• 921440-72-4 5,7-dimethoxy-3-(1-methyl-1H-benzimidazol-2-yl)-2-phenylquinoline 
• 920864-03-5 1,3-dimethyl-6-(1-methyl-1H-benzimidazol-2-yl)-7-phenylpyrido[2,3-d]pyrimidine-2,4-(1H,3H)-dione 

Relevant academic research and scientific papers

The impact of the heteroatom in a five-membered ring on the photophysical properties of difluoroborates

A series of novel BF2 complexes, bearing a five-membered heterocyclic ring (with X = NMe, O, and S), were synthesized and characterized with a focus on the influence of atom exchange on the photophysical properties of both unsubstituted and dim

Tautomeric equilibria in solutions of 1-methyl-2-phenacylbenzimidazoles

Until now the susceptibility of 1-methyl-2-phenacylbenzimidazoles to the proton transfer has not been carefully examined. There only have been selective trials to recognize tautomeric equilibrium of substituted compounds. Unfortunately, conclusions of the

THE SYNTHESIS AND TAUTOMERIZATION OF KETENE AMINALS WITH BENZIMIDAZOLINE RING

The first isolation of benzimidazoline ring substituted ketene aminals 7a-c and/or their amidine tautomers 7'b-d, which were synthesized by the reactions: (1) benzoyl substituted ketene mercaptals 3 with N-methyl-o-phenylenediamine 4, and (2) 1,2-dimethylbenzimidazole 5 with ethyl benzoates 6, were disclosed.The tautomeric equilibrium between 7 and 7', along with benzothiazoline and benzoxazoline ring substituted ketene N,S-acetals 8 and 8' and ketene N,O-acetals 9 and 9', were discussed.