Phenylamino(thiocarbonyl)diphenylphosphine

Base Information

• Chemical Name: Phenylamino(thiocarbonyl)diphenylphosphine
• CAS No.: 739-61-7
• Molecular Formula: C19H16 N P S
• Molecular Weight: 321.383
• NSC Number: 346109,346105
• DSSTox Substance ID: DTXSID10995039
• Nikkaji Number: J1.275.476K

Synonyms:739-61-7;NSC346109;DTXSID10995039;NSC346105;AKOS024371623;NSC-346105;NSC-346109;Phenylamino(thiocarbonyl)diphenylphosphine;N,1,1-Triphenylphosphanecarboximidothioic acid;82449-23-8

Chemical Property of Phenylamino(thiocarbonyl)diphenylphosphine

Chemical Property:

• Vapor Pressure: 2.33E-08mmHg at 25°C
• Boiling Point: 452°C at 760 mmHg
• Flash Point: 227.1°C
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 321.07410769
• Heavy Atom Count: 22
• Complexity: 323

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)NC(=S)P(C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of Phenylamino(thiocarbonyl)diphenylphosphine

There total 3 articles about Phenylamino(thiocarbonyl)diphenylphosphine 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%

phenyl isothiocyanate (103-72-0) + diphenylphosphane (829-85-6) → diphenyl(N-phenylthiocarbamoyl)phosphine (739-61-7)

Guidance literature:

With C₃₄H₅₈N₇Si₄Y; In tetrahydrofuran; at 20 ℃; for 0.5h; Inert atmosphere; Glovebox; Schlenk technique;

DOI:10.1021/acs.organomet.5b00628

Reference yield: 86.0%

N-1,1-triphenyl-N-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phosphinecarbothioamide → diphenyl(N-phenylthiocarbamoyl)phosphine (739-61-7)

Guidance literature:

In methanol; for 0.5h;

DOI:10.1039/c7dt02305g

Reference yield:

→ diphenyl(N-phenylthiocarbamoyl)phosphine (739-61-7)

Guidance literature:

PH(C6H5)2, C6H5NCS;

upstream raw materials:

phenyl isothiocyanate

diphenylphosphane

Downstream raw materials:

S-Methyl-1-(diphenylphosphino)-N-phenylthioformimidat

(CO)5CrP(C₆H₅)2C(S)NHC₆H₅

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