Dimethylheptylpyran

Dimethylheptylpyran
Clinical data
ATC code	none;
Legal status
Legal status	AU: S9 (Prohibited substance); BR: Class F2 (Prohibited psychotropics); DE: Anlage I (Authorized scientific use only); UK: Class B; US: Schedule I; UN: Psychotropic Schedule I;
Pharmacokinetic data
Elimination half-life	20–39 hours
Identifiers
	IUPAC name 6,6,9-Trimethyl-3-(3-methyl-2-octanyl)-7,8,9,10-tetrahydro-6H-benzo[c]chromen-1-ol;
CAS Number	32904-22-6 ;
PubChem CID	36276;
ChemSpider	33359 ;
UNII	944O1KA97G;
KEGG	C22734 ;
ChEMBL	ChEMBL3244434 ;
CompTox Dashboard (EPA)	DTXSID60954555 ;
Chemical and physical data
Formula	C25H38O2
Molar mass	370.577 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCCCCC(C)C(C)c1cc(c2c(c1)OC(C3=C2CC(CC3)C)(C)C)O;
	InChI InChI=1S/C25H38O2/c1-7-8-9-10-17(3)18(4)19-14-22(26)24-20-13-16(2)11-12-21(20)25(5,6)27-23(24)15-19/h14-18,26H,7-13H2,1-6H3 ; Key:QBEFIFWEOSUTKV-UHFFFAOYSA-N ;
	(what is this?) (verify)

Dimethylheptylpyran (DMHP, 3-(1,2-dimethylheptyl)-Δ^6a(10a)-THC, 1,2-dimethylheptyl-Δ³-THC, A-40824, or EA-2233) is a synthetic analog of THC, which was invented in 1949 during attempts to elucidate the structure of Δ⁹-THC, one of the active components of Cannabis. DMHP is a pale yellow, viscous oil which is insoluble in water but dissolves in alcohol or non-polar solvents.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.