2-Methoxybenzyl methyl sulfide

Base Information

Chemical Name:2-Methoxybenzyl methyl sulfide
CAS No.:81077-60-3
Molecular Formula:C₉H₁₂OS
Molecular Weight:168.26
Hs Code.:
European Community (EC) Number:666-116-4
Nikkaji Number:J1.105.449H

Synonyms:2-Methoxybenzyl methyl sulfide;81077-60-3;1-methoxy-2-[(methylsulfanyl)methyl]benzene;(methylthiomethyl)anisole;SCHEMBL515180;Methyl 2-methoxybenzyl sulfide;AKOS024324155;1-methoxy-2-[(methylthio)methyl]benzene

Suppliers and Price of 2-Methoxybenzyl methyl sulfide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of 2-Methoxybenzyl methyl sulfide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:168.06088618
Heavy Atom Count:11
Complexity:106

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC=CC=C1CSC

Technology Process of 2-Methoxybenzyl methyl sulfide

There total 1 articles about 2-Methoxybenzyl methyl sulfide 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:

: 16437-69-7
(methylthio)methyl acetate

: 100-66-3
methoxybenzene

: 1618-26-4
2,4-dithiapentane

: 5925-86-0
(4-methoxybenzyl)methylsulfide

: 104-21-2
p-methoxybenzyl acetate

: 81077-60-3
o-methylthiomethylanisole

Guidance literature:: With boron trifluoride diethyl etherate; at 100 ℃; for 3h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1039/P19810003070