Marmesin

Marmesin
IUPAC name (2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one
Identifiers
CAS number	13849-08-6
PubChem	334704
ChemSpider	296611
Jmol-3D images	{{#if:CC(C)([C@@H]1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O|Image 1
SMILES CC(C)([C@@H]1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O
InChI InChI=InChI=1S/C14H14O4/c1-14(2, 16)12-6-9-5-8-3-4-13(15)18-10(8)7-11(9)17-12/h3-5,7,12,16H,6H2, 1-2H3/t12-/m0/s1 Key: FWYSBEAFFPBAQU-LBPRGKRZSA-N
Properties
Molecular formula	C14H14O4
Molar mass	246.26 g mol−1
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Marmesin is a chemical compound precursor in psoralen and linear furanocoumarins biosynthesis.^[1]

References

1. ↑ Steck, Warren; Brown, Stewart A. (1971). "Comparison of (+)- and (−)-Marmesin as Intermediates in the Biosynthesis of Linear Furanoconmarins". Biochemistry and Cell Biology 49 (11): 1213–1216. doi:10.1139/o71-174. ISSN 1208-6002. 

Bibliography

• Jain, Mahendra (2010). "TLC Determination of Marmesin, a Biologically Active Marker from Feronia Limonia L.". American Journal of Plant Sciences 01 (01): 12–16. doi:10.4236/ajps.2010.11002. ISSN 2158-2742. 
• Abu-Mustafa, Effat A.; Fayez, M. B. E. (1961). "Natural Coumarins. I. Marmesin and Marmesinin, Further Products from the Fruits of Ammi majus L.". The Journal of Organic Chemistry 26 (1): 161–166. doi:10.1021/jo01060a039. ISSN 0022-3263.