[3,4,5-Trimethoxy-2-(methylsulfanylmethyl)phenyl]methanol

Base Information

Chemical Name:[3,4,5-Trimethoxy-2-(methylsulfanylmethyl)phenyl]methanol
CAS No.:124867-99-8
Molecular Formula:C₁₂H₁₈O₄S
Molecular Weight:258.339
Hs Code.:
DSSTox Substance ID:DTXSID801347772
Nikkaji Number:J182.752I
Wikidata:Q63409815

Synonyms:124867-99-8;DTXSID801347772;Q63409815;3,4,5-TRIMETHOXY-2-METHYLTHIOMETHYLBENZYLALCOHOL;{3,4,5-Trimethoxy-2-[(methylsulfanyl)methyl]phenyl}methanol

Suppliers and Price of [3,4,5-Trimethoxy-2-(methylsulfanylmethyl)phenyl]methanol

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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 [3,4,5-Trimethoxy-2-(methylsulfanylmethyl)phenyl]methanol

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:258.09258022
Heavy Atom Count:17
Complexity:215

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C(=C(C(=C1)CO)CSC)OC)OC

Technology Process of [3,4,5-Trimethoxy-2-(methylsulfanylmethyl)phenyl]methanol

There total 2 articles about [3,4,5-Trimethoxy-2-(methylsulfanylmethyl)phenyl]methanol 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: 87.0%

: 124867-98-7
2-methylthiomethyl-3,4,5-trimethoxybenzoate

: 124867-99-8
2-methylthiomethyl-3,4,5-trimethoxybenzyl alcohol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 2h; Ambient temperature;
DOI:10.1246/bcsj.62.2427

Reference yield:

: 1916-07-0
3,4,5-trimethoxybenzoic acid methyl ester

: 124867-99-8
2-methylthiomethyl-3,4,5-trimethoxybenzyl alcohol

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / SnCl₄ / CH₂Cl₂ / 7 h / Ambient temperature

2: 87 percent / LiAlH₄ / diethyl ether / 2 h / Ambient temperature

With lithium aluminium tetrahydride; tin(IV) chloride; In diethyl ether; dichloromethane;
DOI:10.1246/bcsj.62.2427