(1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

Base Information

Chemical Name:(1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione
CAS No.:714217-53-5
Molecular Formula:C₃₀H₄₅IO₇
Molecular Weight:644.588
Hs Code.:

(1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

Synonyms:(1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

Suppliers and Price of (1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

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Chemical Property of (1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

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Technology Process of (1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

There total 1 articles about (1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 57.0%

: 64761-29-1
mesitaldehyde dimethylacetal

: 116417-70-0
(8S)-8,8a-deepoxy-8-hydroxy-8a-iodooleandonolide

: 714217-53-5
(1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

Guidance literature:: With camphor-10-sulfonic acid; In dichloromethane; at 20 ℃; for 6h;
DOI:10.1016/j.tet.2004.03.061

Reference yield:

: 714217-53-5
(1S,2R,5R,6R,7S,8R,10S,12S,13S,15S,17R)-7,10-Dihydroxy-10-iodomethyl-2,5,6,8,12,17-hexamethyl-15-(2,4,6-trimethyl-phenyl)-4,14,16-trioxa-bicyclo[11.3.1]heptadecane-3,9-dione

: 714217-46-6
(9R)-9-dihydro-3,5-O-(2,4,6-trimethylbenzylidene)-oleandonolide

Guidance literature:: With sodium tetrahydroborate; In ethyl acetate; isopropyl alcohol; at 20 ℃; for 0.333333h;
DOI:10.1016/S0040-4039(03)00954-7