(2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol

Base Information

Chemical Name:(2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol
CAS No.:1046471-46-8
Molecular Formula:C₂₀H₃₂O₅
Molecular Weight:352.471
Hs Code.:

Synonyms:(2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol

Suppliers and Price of (2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol

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Technology Process of (2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol

There total 1 articles about (2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol 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: 100.0%

: 1046471-29-7
(2S,3S,4S,6S)-7-(tert-butyldiphenylsilyloxy)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethylheptane

: 1046471-46-8
(2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ol801395q

Reference yield: 93.0%

: 1046471-46-8
(2S,3S,4S,6S)-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethyl-7-heptanol

: 1046471-22-0
(2S,3S,4S,6S)-7-bromo-3,4-O-isopropylidene-1-(4-methoxybenzyloxy)-2,6-dimethylheptane

Guidance literature:: With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1021/ol801395q