Α-Chlorocodide

α-Chlorocodide
Names
	IUPAC name (5α,6β)-6-Chloro-3-methoxy-17-methyl-7,8-didehydro-4,5-epoxymorphinan
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	4588984;
PubChem CID	5486612;
CompTox Dashboard (EPA)	DTXSID10963637 ;
	InChI InChI=1S/C18H20ClNO2/c1-20-8-7-18-11-4-5-12(19)17(18)22-16-14(21-2)6-3-10(15(16)18)9-13(11)20/h3-6,11-13,17H,7-9H2,1-2H3/t11-,12+,13+,17-,18-/m0/s1 Key: CVLHOXTTXWEUCL-KEMUOJQUSA-N; InChI=1/C18H20ClNO2/c1-20-8-7-18-11-4-5-12(19)17(18)22-16-14(21-2)6-3-10(15(16)18)9-13(11)20/h3-6,11-13,17H,7-9H2,1-2H3/t11-,12+,13+,17-,18-/m0/s1 Key: CVLHOXTTXWEUCL-KEMUOJQUBZ;
	SMILES Cl[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	C18H20ClNO2
Molar mass	317.81 g·mol−1
Melting point	151 to 154 °C (304 to 309 °F; 424 to 427 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

α-Chlorocodide is an opioid analog that is a derivative of codeine in which the 6-hydroxy group has been replaced by chlorine.

References

^ Stork, Gilbert; Clarke, Frank H. (1956). "The SN2' Reaction. III. Structure and SN2' Reactions of the Halocodides". Journal of the American Chemical Society. 78 (18): 4619–4624. doi:10.1021/ja01599a026.

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