Dibenzyl sulfate

Base Information

Chemical Name:Dibenzyl sulfate
CAS No.:18495-74-4
Molecular Formula:C14H14O4S
Molecular Weight:278.329
Hs Code.:
DSSTox Substance ID:DTXSID60556119
Mol file:18495-74-4.mol

Synonyms:dibenzyl sulfate;18495-74-4;Sulfuric acid, bis(phenylmethyl) ester;Dibenzylsulfat;SCHEMBL561014;DTXSID60556119;A936573

Suppliers and Price of Dibenzyl sulfate

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 Dibenzyl sulfate

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:278.06128010
Heavy Atom Count:19
Complexity:307

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COS(=O)(=O)OCC2=CC=CC=C2

Technology Process of Dibenzyl sulfate

There total 1 articles about Dibenzyl sulfate 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:

: 138337-14-1
potassium N-Nitroso-N-benzylsulfamate

: 65-85-0,8013-63-6
benzoic acid

: 120-51-4
benzoic acid benzyl ester

: 18687-57-5
potassium benzyl sulfate

: 18495-74-4
dibenzyl sulfate

: 100-51-6,185532-71-2
benzyl alcohol

Guidance literature:: In diethyl ether; for 4h; Ambient temperature; other trapping agents;
DOI:10.1021/jo00030a037

Reference yield: 69.0%

: C₂₇H₁₇BrN₄O

: 18495-74-4
dibenzyl sulfate

: C₃₄H₂₃BrN₄O

Guidance literature:: With tetrabutylammomium bromide; potassium carbonate; In acetonitrile; at 20 ℃; for 3h;
DOI:10.2174/1570180816666191024103534