4-Methoxybenzyl thiocyanate

Base Information

Chemical Name:4-Methoxybenzyl thiocyanate
CAS No.:19927-28-7
Molecular Formula:C9H9NOS
Molecular Weight:179.243
Hs Code.:
DSSTox Substance ID:DTXSID701033831
Nikkaji Number:J338.271K

Synonyms:4-Methoxybenzyl thiocyanate;19927-28-7;(4-methoxyphenyl)methyl thiocyanate;Thiocyanic acid, (4-methoxyphenyl)methyl ester;SCHEMBL12695885;DTXSID701033831;GEO-02683;AKOS006291307;{[(4-methoxyphenyl)methyl]sulfanyl}carbonitrile

Suppliers and Price of 4-Methoxybenzyl thiocyanate

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
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price

Total 1 raw suppliers

Chemical Property of 4-Methoxybenzyl thiocyanate

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:179.04048508
Heavy Atom Count:12
Complexity:167

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC=C(C=C1)CSC#N

Technology Process of 4-Methoxybenzyl thiocyanate

There total 30 articles about 4-Methoxybenzyl thiocyanate 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%

: ammonium thiocyanate

: 105-13-5
4-Methoxybenzyl alcohol

: 19927-28-7
p-methoxybenzyl thiocyanate

Guidance literature:: ammonium thiocyanate; With 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octanebis(tetrafluoroborate); In acetonitrile; at 20 ℃; for 0.333333h;

4-Methoxybenzyl alcohol; In acetonitrile; for 0.05h;
DOI:10.1016/j.jfluchem.2012.03.005