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1,1'-(4-Chlorobutylidene)bisbenzene

Base Information Edit
  • Chemical Name:1,1'-(4-Chlorobutylidene)bisbenzene
  • CAS No.:3312-08-1
  • Molecular Formula:C16H17 Cl
  • Molecular Weight:244.764
  • Hs Code.:2903999090
  • European Community (EC) Number:221-999-1
  • DSSTox Substance ID:DTXSID50186782
  • Nikkaji Number:J205.393D
  • Wikidata:Q83058175
  • Mol file:3312-08-1.mol
1,1'-(4-Chlorobutylidene)bisbenzene

Synonyms:1,1'-(4-Chlorobutylidene)bisbenzene;3312-08-1;(4-chloro-1-phenylbutyl)benzene;EINECS 221-999-1;1,1-diphenyl-4-chlorobutane;1-chloro-4,4-diphenylbutane;4-Chloro-1,1-diphenylbutane;SCHEMBL5635206;DTXSID50186782

Suppliers and Price of 1,1'-(4-Chlorobutylidene)bisbenzene
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 3 raw suppliers
Chemical Property of 1,1'-(4-Chlorobutylidene)bisbenzene Edit
Chemical Property:
  • Boiling Point:362.5oC at 760 mmHg 
  • Flash Point:164.6oC 
  • PSA:0.00000 
  • Density:1.061g/cm3 
  • LogP:4.83750 
  • XLogP3:4.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:5
  • Exact Mass:244.1018782
  • Heavy Atom Count:17
  • Complexity:172
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(CCCCl)C2=CC=CC=C2
Technology Process of 1,1'-(4-Chlorobutylidene)bisbenzene

There total 3 articles about 1,1'-(4-Chlorobutylidene)bisbenzene 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:
Guidance literature:
With hydrogen; palladium on activated charcoal; In isopropyl alcohol;
Guidance literature:
With n-butyllithium; Yield given. Multistep reaction; 1.) THF-hexane, 23 deg C, 15 min, 2.) THF, from -78 to 23 deg C, 30 min;
Guidance literature:
entspr. Cyclopropylcarbinol, HX, H2;
Refernces Edit
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