(1,2-Dichloro-1,2,2-triphenylethyl)benzene

Base Information

• Chemical Name: (1,2-Dichloro-1,2,2-triphenylethyl)benzene
• CAS No.: 1600-30-2
• Molecular Formula: C26H20 Cl2
• Molecular Weight: 403.351
• NSC Number: 133268,40471
• DSSTox Substance ID: DTXSID60285098
• Nikkaji Number: J600.824K
• Wikidata: Q82020346
• Mol file: 1600-30-2.mol

Synonyms:(1,2-dichloro-1,2,2-triphenylethyl)benzene;1600-30-2;1,1',1'',1'''-(1,2-dichloroethane-1,1,2,2-tetrayl)tetrabenzene;NSC40471;1,2-dichlorotetra-phenylethane;SCHEMBL10940043;DTXSID60285098;NSC-40471;NSC133268;AKOS024428868;NSC-133268

Chemical Property of (1,2-Dichloro-1,2,2-triphenylethyl)benzene

Chemical Property:

• XLogP3: 7.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 5
• Exact Mass: 402.0942060
• Heavy Atom Count: 28
• Complexity: 383

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)C(C2=CC=CC=C2)(C(C3=CC=CC=C3)(C4=CC=CC=C4)Cl)Cl

Technology Process of (1,2-Dichloro-1,2,2-triphenylethyl)benzene

There total 15 articles about (1,2-Dichloro-1,2,2-triphenylethyl)benzene 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: 52.0%

Dichlorodiphenylmethane (2051-90-3) → 1,2-dichloro-1,1,2,2-tetraphenylethane (1600-30-2) + 1,1,2,2-tetraphenylethylene (632-51-9)

Guidance literature:

With CrCl*nTHF; In tetrahydrofuran; at 25 ℃; for 12h;

DOI:10.1002/cber.19971300903

Reference yield:

phosphorus pentachloride (10026-13-8,874483-75-7) + benzophenone azine monoxide (7463-87-8) → benzophenone (119-61-9) + 1,2-dichloro-1,1,2,2-tetraphenylethane (1600-30-2)

Guidance literature:

at 0 ℃; oberhalb 0grad erfolgt Verpuffung;

Reference yield:

1,1,2,2-tetraphenylethylene (632-51-9) → 1,2-dichloro-1,1,2,2-tetraphenylethane (1600-30-2)

Guidance literature:

With tetrachloromethane; chlorine;

upstream raw materials:

Dichlorodiphenylmethane

1,1,2,2-tetraphenylethylene

benzophenone azine

tetraphenylethane-1,2-diol

Downstream raw materials:

benzopinacolone

tetraphenyloxirane

1,1,2,2-tetraphenylethylene

(2-(4-chlorophenyl)ethene-1,1,2-triyl)tribenzene