Isocodeine

Isocodeine
Names
	IUPAC name (5α,6β)-3-Methoxy-17-methyl-7,8-didehydro-4,5-epoxymorphinan-6-ol
	Other names 6-Isocodeine; α-Isocodeine
Identifiers
CAS Number	509-64-8 ;
3D model (JSmol)	Interactive image;
ChemSpider	4481821;
ECHA InfoCard	100.007.366
EC Number	208-101-3;
PubChem CID	5324288;
CompTox Dashboard (EPA)	DTXSID10858973 ;
	InChI InChI=1S/C18H21NO3/c1-19-8-7-18-11-4-5-13(20)17(18)22-16-14(21-2)6-3-10(15(16)18)9-12(11)19/h3-6,11-13,17,20H,7-9H2,1-2H3/t11-,12+,13+,17-,18-/m0/s1 Key: OROGSEYTTFOCAN-KEMUOJQUSA-N; InChI=1/C18H21NO3/c1-19-8-7-18-11-4-5-13(20)17(18)22-16-14(21-2)6-3-10(15(16)18)9-12(11)19/h3-6,11-13,17,20H,7-9H2,1-2H3/t11-,12+,13+,17-,18-/m0/s1 Key: OROGSEYTTFOCAN-KEMUOJQUBO;
	SMILES O[C@@H]2\C=C/[C@H]5[C@@H]4N(CC[C@@]51c3c(O[C@H]12)c(OC)ccc3C4)C;
Properties
Chemical formula	C18H21NO3
Molar mass	299.370 g·mol−1
Melting point	173 to 174 °C (343 to 345 °F; 446 to 447 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H301, H302, H331
Precautionary statements	P261, P264, P270, P271, P301+P310, P301+P312, P304+P340, P311, P321, P330, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Isocodeine is an opioid research chemical related to codeine. It is an epimer of codeine that can be prepared from it by a Mitsunobu reaction.^[1]

Dozens of derivatives and analogs of isocodeine and the related compound isomorphine have been produced.^[2] One of these, dihydroisocodeine is a pharmaceutical four times stronger than dihydrocodeine and thus six times stronger than codeine which was used more extensively in the past in Continental Europe and other locales. Other isomers of codeine include allocodeine, pseudocodeine, heterocodeine and substances with intermediate qualities such as pseudoallocodeine and formylallocodeine can be prepared in the laboratory.^[3]

References

^ ^a ^b Simon, Csaba; Hosztafi, Sándor; Makleit, Sándor (1991). "Application of the Mitsunobu Reaction for the Preparation of Isomorphine and Isocodeine Derivatives". Synthetic Communications. 21 (3): 407–412. doi:10.1080/00397919108016763.
^ "Report of Committee on drug addiction, 1929-1941" (Document). National Research Council (US).
^ Report of the Committee On Drug Addiction 1929-1941 with Monographs, 1941, National Research Council (US) Washington DC, 1116 pages (Chapter 7)

This analgesic-related article is a stub. You can help Wikipedia by expanding it.

[Simon-1] Simon, Csaba; Hosztafi, Sándor; Makleit, Sándor (1991). "Application of the Mitsunobu Reaction for the Preparation of Isomorphine and Isocodeine Derivatives". Synthetic Communications. 21 (3): 407–412. doi:10.1080/00397919108016763.

[2] "Report of Committee on drug addiction, 1929-1941" (Document). National Research Council (US).

[3] Report of the Committee On Drug Addiction 1929-1941 with Monographs, 1941, National Research Council (US) Washington DC, 1116 pages (Chapter 7)

[1]

[2]

[3]