tert-Butyl(phenyl)phosphinic isothiocyanate

Base Information Edit

Chemical Name:tert-Butyl(phenyl)phosphinic isothiocyanate
CAS No.:54100-46-8
Molecular Formula:C₁₁H₁₄NOPS
Molecular Weight:239.278
Hs Code.:
DSSTox Substance ID:DTXSID10507070
Mol file:54100-46-8.mol

Synonyms:54100-46-8;tert-Butyl(phenyl)phosphinic isothiocyanate;DTXSID10507070

Suppliers and Price of tert-Butyl(phenyl)phosphinic isothiocyanate

Supply Marketing:Edit

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of tert-Butyl(phenyl)phosphinic isothiocyanate Edit

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:239.05337224
Heavy Atom Count:15
Complexity:309

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)P(=O)(C1=CC=CC=C1)N=C=S

Technology Process of tert-Butyl(phenyl)phosphinic isothiocyanate

There total 13 articles about tert-Butyl(phenyl)phosphinic isothiocyanate 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: 88.0%

: 7677-24-9
trimethylsilyl cyanide

: 64578-97-8
Bis-disulfid

: 54100-46-8
tert-butylphenylphosphinoyl isothiocyanate

: 115255-55-5
C₁₃H₂₃OPSSi

Guidance literature:: In dichloromethane; Ambient temperature;

Reference yield: 87.0%

: 1147550-11-5
ammonium thiocyanate

: 82220-43-7,82220-48-2
tert-butylphenylphosphinic methanesulfonic anhydride

: 54100-46-8
tert-butylphenylphosphinoyl isothiocyanate

Guidance literature:: In diethyl ether; for 12h; Ambient temperature; further educts: tert-butylphenylphosphinic trifluoromethanesulfonic, -imidazolidosulfuric, -4-methylbenzenesulfonic anhydrides;