Triphenyllead chloride

Base Information

• Chemical Name: Triphenyllead chloride
• CAS No.: 1153-06-6
• Molecular Formula: C18H15 Cl Pb
• Molecular Weight: 473.97
• Hs Code.: 2931900090
• European Community (EC) Number: 214-572-6
• NSC Number: 12104
• DSSTox Substance ID: DTXSID201033793
• Mol file: 1153-06-6.mol

Synonyms:TPhL chloride;triphenyllead chloride

Chemical Property of Triphenyllead chloride

Chemical Property:

• Vapor Pressure: 2.32E-07mmHg at 25°C
• Melting Point: 207oC(lit.)
• Boiling Point: 434.9°Cat760mmHg
• Flash Point: 216.8°C
• PSA: 0.00000
• Density: g/cm³
• LogP: 4.76910
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 474.06288
• Heavy Atom Count: 20
• Complexity: 240

Purity/Quality:

98%,99%, ^*data from raw suppliers

CHLOROTRIPHENYLLEAD(IV) 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T,N
• Hazard Codes: T,N
• Statements: 61-20/22-33-50/53-62
• Safety Statements: 53-45-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC=C(C=C1)[Pb](C2=CC=CC=C2)(C3=CC=CC=C3)Cl

Technology Process of Triphenyllead chloride

There total 118 articles about Triphenyllead chloride 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%

4,4,4-Trifluoro-1-phenyl-2-(triphenyl-λ5-arsanylidene)-butane-1,3-dione (91529-28-1,91529-31-6) → 1-Phenyl-4,4,4-trifluorobutane-1,3-dione (326-06-7) + triphenylarsineoxide (1153-05-5,856568-31-5)

Guidance literature:

With hydrogenchloride; In dichloromethane; Product distribution;

DOI:10.1007/BF00995718

Reference yield: 96.0%

triphenyl-arsane (603-32-7) → triphenylarsineoxide (1153-05-5,856568-31-5)

Guidance literature:

With macroporous polystyrene-supported (diacetoxyiodo)benzene; In tetrahydrofuran; at 20 ℃; for 4h;

DOI:10.1055/s-2006-958450

Reference yield: 94.0%

dimeric N-(o-methoxyphenyl)-As,As,As-triphenylarsine imide hydrochloride → triphenylarsineoxide (1153-05-5,856568-31-5) + 2-methoxyaniline hydrochloride (134-29-2) + hydroxytriphenylarsonium chloride

Guidance literature:

With water; for 2h; Product distribution; Heating; different reaction conditions of hydrolysis;

upstream raw materials:

trimethylamine hydrochloride

Tetraphenyllead

hydrogenchloride

chloroform

Downstream raw materials:

Tetraphenyllead

hexa-Pb-phenyl-Pb,Pb'-p-phenylene-bis plumbane

phenylmercury(II) chloride

triphenyl-styryl plumbane

Refernces

• 1、 Ibdah, Abdellatif,Bakar, Heba Bani,Alduwikat, Salwa. "Kinetic and Computational Studies of Rhenium Catalysis for Oxygen Atom Transfer Reactions". . p. 149 - 159. Retrieved 2018/03/09.
• 2、 El-Sayed, Naglaa F.,Ewies, Ewies F.,El-Hussieny, Marwa,Boulos, Leila S.,Shalaby, ElSayed M.. "Synthesis of novel pyrazole derivatives using organophosphorus, stibine, and arsine reagents and their antitumor activities". . p. 765 - 776. Retrieved 2016/07/27.