Benzoylthiomethylecgonine

Benzoylthiomethylecgonine

Identifiers
CAS Registry Number	287488-21-5 Y
ChemSpider	26286895
InChI InChI=1S/C17H21NO3S/c1-18-12-8-9-13(18)15(16(19)21-2)14(10-12)22-17(20)11-6-4-3-5-7-11/h3-7,12-15H,8-10H2,1-2H3/t12-,13+,14-,15+/m0/s1 Key: PKDHUFYOPRGLEU-LJISPDSOSA-N InChI=1/C17H21NO3S/c1-18-12-8-9-13(18)15(16(19)21-2)14(10-12)22-17(20)11-6-4-3-5-7-11/h3-7,12-15H,8-10H2,1-2H3/t12-,13+,14-,15+/m0/s1 Key: PKDHUFYOPRGLEU-LJISPDSOBR
Jmol-3D images	Image
SMILES CN1[C@H]2CC[C@@H]1[C@H]([C@H](C2)SC(=O)c3ccccc3)C(=O)OC
Properties
Molecular formula	C17H21NO3S
Molar mass	319.42 g·mol−1
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Benzoylthiomethylecgonine is a cocaine analog which includes a sulfur in replacement of an oxygen on the single bonded benzoyl ester, resulting in lower electronegativity than the parent compound.^[1]

See also

• Salicylmethylecgonine
• 2'-Acetoxycocaine
• 4'-Fluorococaine

References

1. ↑ Isomura, Shigeki; Hoffman, Timothy Z.; Wirsching, Peter; Janda, Kim D. (2002). "Synthesis, Properties, and Reactivity of Cocaine Benzoylthio Ester Possessing the Cocaine Absolute Configuration". Journal of the American Chemical Society 124 (14): 3661–8. doi:10.1021/ja012376y. PMID 11929256.