|
|
| | 4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl β-D-glucopyranoside 6-[3-(4-hydroxyphenyl)propenoate] Basic information |
| Product Name: | 4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl β-D-glucopyranoside 6-[3-(4-hydroxyphenyl)propenoate] | | Synonyms: | 4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl β-D-glucopyranoside 6-[3-(4-hydroxyphenyl)propenoate];Ipomine;β-D-Glucopyranoside, 4-[(8aS)-1,2,3,5,8,8a-hexahydro-7-methyl-6-indolizinyl]phenyl, 6-[(2E)-3-(4-hydroxyphenyl)-2-propenoate] (9CI) | | CAS: | 65370-71-0 | | MF: | C30H35NO8 | | MW: | 537.6 | | EINECS: | | | Product Categories: | | | Mol File: | 65370-71-0.mol | ![4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl β-D-glucopyranoside 6-[3-(4-hydroxyphenyl)propenoate] Structure](CAS/20180808/GIF/65370-71-0.gif) |
| | 4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl β-D-glucopyranoside 6-[3-(4-hydroxyphenyl)propenoate] Chemical Properties |
| | 4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl β-D-glucopyranoside 6-[3-(4-hydroxyphenyl)propenoate] Usage And Synthesis |
| Occurrence | Ipomoea muricata yields this glycoalkaloid. It forms an
amorphous solid from Et20 having a fairly sharp melting point. The base is dextrorotatory
with a specific rotation of [α]D +46.4° (CHCI3) and gives an ultraviolet spectrum in EtOH
with absorption maxima at 232 and 315 nm. lpomine has been characterized as the picrate,
m.p. 138-141°C. |
| | 4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl β-D-glucopyranoside 6-[3-(4-hydroxyphenyl)propenoate] Preparation Products And Raw materials |
|