Methylecgonine cinnamate

Names
IUPAC name methyl (1R,2R,3S,5S)-8-methyl-3-[(E)-3-phenylprop-2-enoyl]oxy-8-azabicyclo[3.2.1]octane-2-carboxylate
Other names Cinnamoylcocaine Cinnamylcocaine
Identifiers
CAS Number	50763-20-7 Y 521-67-5 (non-specific) Y
3D model (JSmol)	Interactive image
ChemSpider	16735745 Y
PubChem CID	6440936
UNII	O3I44O988U Y
CompTox Dashboard (EPA)	DTXSID60893899
InChI InChI=1S/C19H23NO4/c1-20-14-9-10-15(20)18(19(22)23-2)16(12-14)24-17(21)11-8-13-6-4-3-5-7-13/h3-8,11,14-16,18H,9-10,12H2,1-2H3/b11-8+/t14?,15?,16?,18-/m1/s1 Y Key: MQIXMJWNEKUAOZ-GKMMPQBVSA-N Y InChI=1/C19H23NO4/c1-20-14-9-10-15(20)18(19(22)23-2)16(12-14)24-17(21)11-8-13-6-4-3-5-7-13/h3-8,11,14-16,18H,9-10,12H2,1-2H3/b11-8+/t14?,15?,16?,18-/m1/s1 Key: MQIXMJWNEKUAOZ-GKMMPQBVBP
SMILES CN3C2CCC3CC(OC(=O)/C=C/c1ccccc1)[C@@H]2C(=O)OC
Properties
Chemical formula	C19H23NO4
Molar mass	329.396 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Methylecgonine cinnamate is a natural tropane alkaloid found within the coca plant.^[1] Its more common name, cinnamoylcocaine, reflects its close structural similarity to cocaine. It is pharmacologically inactive,^[2] but some studies funded by anti-drug agencies imply that it is active when smoked.^{[citation needed]} Furthermore, the discovery of differing impurity products yielding methylecgonine cinnamate in confiscated cocaine have led enforcing agencies to postulate that illicit manufacturers have changed their oxidation procedures when refining cocaine from a crude form.^[3] Methylecgonine cinnamate can dimerize to the truxillic acid derivative truxilline.^[2] It is notable that methylecgonine cinnamate is given in patents of active cocaine analogue structures.^[4][5]