Phosphonamidothioic acid, N-(1,1-dimethylethyl)-P-phenyl-

Base Information

Chemical Name:Phosphonamidothioic acid, N-(1,1-dimethylethyl)-P-phenyl-
CAS No.:116762-41-5
Molecular Formula:C₁₀H₁₆NOPS
Molecular Weight:229.283
Hs Code.:
DSSTox Substance ID:DTXSID50479181
Nikkaji Number:J1.119.899F
Mol file:116762-41-5.mol

Synonyms:116762-41-5;Phosphonamidothioic acid, N-(1,1-dimethylethyl)-P-phenyl-;DTXSID50479181

Suppliers and Price of Phosphonamidothioic acid, N-(1,1-dimethylethyl)-P-phenyl-

Supply Marketing:

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

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Chemical Property of Phosphonamidothioic acid, N-(1,1-dimethylethyl)-P-phenyl-

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:229.06902231
Heavy Atom Count:14
Complexity:231

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)NP(=S)(C1=CC=CC=C1)O

Technology Process of Phosphonamidothioic acid, N-(1,1-dimethylethyl)-P-phenyl-

There total 4 articles about Phosphonamidothioic acid, N-(1,1-dimethylethyl)-P-phenyl- 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: 71.0%

: 116762-44-8
racemic N-t-butyl-P-phenylphosphonamidothioic chloride

: 116762-41-5,230958-73-3
racemic N-t-butyl-P-phenylphosphonamidothioic acid

Guidance literature:: With sodium hydroxide;
DOI:10.1039/P29880000081

Reference yield:

: 644-97-3
Dichlorophenylphosphine

: 116762-41-5,230958-73-3
racemic N-t-butyl-P-phenylphosphonamidothioic acid

Guidance literature:: Multi-step reaction with 3 steps

1: benzene / 1.) 0.5 h, 0-5 deg C; 2.) 0.5 h, RT

2: sulphur / benzene / 23 h / Heating

3: 71 percent / 2 M NaOH

With sodium hydroxide; sulfur; In benzene;
DOI:10.1039/P29880000081

Reference yield:

: 95980-86-2
t-butylamino-chlorophenylphosphane

: 116762-41-5,230958-73-3
racemic N-t-butyl-P-phenylphosphonamidothioic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sulphur / benzene / 23 h / Heating

2: 71 percent / 2 M NaOH

With sodium hydroxide; sulfur; In benzene;
DOI:10.1039/P29880000081