((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene

Base Information

Chemical Name:((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene
CAS No.:117708-47-1
Molecular Formula:C₁₈H₂₈O₆
Molecular Weight:340.417
Hs Code.:

Synonyms:((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene

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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 ((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene

Chemical Property:

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Technology Process of ((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene

There total 2 articles about ((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene 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:

: 74-88-4
methyl iodide

: 754197-54-1
(1R,2S,3S,4S,5S,6S)-5-Benzyloxy-6-methoxy-cyclohexane-1,2,3,4-tetraol

: 117708-47-1
((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.carres.2004.05.016

Reference yield:

: 68738-30-7
1L-1-O-benzyl-myo-inositol

: 74-88-4
methyl iodide

: 117708-47-1
((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene

Guidance literature:: With sodium methylsulfinylmethanide; In dimethyl sulfoxide; for 1h;
DOI:10.1016/S0008-6215(00)90816-4

Reference yield:

: 117708-47-1
((1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentamethoxy-cyclohexyloxymethyl)-benzene

: 755023-78-0
1D-O¹,O²,O⁴,O⁵,O⁶-pentamethyl-myo-inositol

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 45h; Yield given; Ambient temperature;
DOI:10.1016/S0008-6215(00)90816-4