Differs structurally from 1'-naphthoyl indole by having a methyl group attached at the two position of the indole ring; intended for forensic and research applications

1′-Naphthoyl-2-methylindole – 5 mg

Brand:
Cayman
CAS:
80749-33-3
Storage:
-20
UN-No:
Non-Hazardous - /

A large number of synthetic cannabinoids (CBs) have been detected in herbal blends sold for recreational use.{19508} 1’-Naphthoyl indole represents the simplest form of this group of cannabimimetics. While the addition of an N-alkyl chain of four or more carbons generates compounds which potently activate CB receptors, short chain lengths are inactive at both central CB1 and peripheral CB2.{16797} This suggests that 1’-naphthoyl indole should have no appreciable affinity for either receptor. 1’-Naphthoyl-2-methylindole differs structurally from 1’-naphthoyl indole by having a methyl group attached at the two position of the indole ring. The biological activities of this compound have not been characterized. This product is intended for forensic and research applications.  

 

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Description

Differs structurally from 1′-naphthoyl indole by having a methyl group attached at the two position of the indole ring; intended for forensic and research applications

Formal name: (2-methyl-1H-indol-3-yl)-1-naphthalenyl-methanone

Synonyms: 

Molecular weight: 285.4

CAS: 80749-33-3

Purity: ≥98%

Formulation: A crystalline solid

Application|Mass Spectrometry||Product Type|Biochemicals|Analytical Standards||Product Type|Biochemicals|Drugs of Abuse||Research Area|Forensic Chemistry & Toxicology|Cannabinoids|Synthetic Cannabinoids

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