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1,1-Diphenylbutane

Base Information Edit
  • Chemical Name:1,1-Diphenylbutane
  • CAS No.:719-79-9
  • Molecular Formula:C16H18
  • Molecular Weight:210.319
  • Hs Code.:
  • DSSTox Substance ID:DTXSID3061053
  • Nikkaji Number:J219.546A
  • Wikidata:Q81989284
  • Mol file:719-79-9.mol
1,1-Diphenylbutane

Synonyms:1,1-Diphenylbutane;719-79-9;1-phenylbutylbenzene;Benzene, 1,1'-butylidenebis-;diphenylbutane;Ceanothicacid;(1-Phenylbutyl)benzene;Butane, 1,1-diphenyl-;butane-1,1-diyldibenzene;(1-Phenylbutyl)benzene #;DTXSID3061053;FT-0606149

Suppliers and Price of 1,1-Diphenylbutane
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
  • American Custom Chemicals Corporation
  • 1,1-DIPHENYLBUTANE 95.00%
  • 5MG
  • $ 497.26
Total 3 raw suppliers
Chemical Property of 1,1-Diphenylbutane Edit
Chemical Property:
  • Vapor Pressure:0.0044mmHg at 25°C 
  • Melting Point:-25.2°C 
  • Refractive Index:1.5546 
  • Boiling Point:287°C at 760 mmHg 
  • Flash Point:136.8°C 
  • PSA:0.00000 
  • Density:0.959g/cm3 
  • LogP:4.61860 
  • XLogP3:5.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:4
  • Exact Mass:210.140850574
  • Heavy Atom Count:16
  • Complexity:155
Purity/Quality:

98%Min *data from raw suppliers

1,1-DIPHENYLBUTANE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCC(C1=CC=CC=C1)C2=CC=CC=C2
Technology Process of 1,1-Diphenylbutane

There total 51 articles about 1,1-Diphenylbutane 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 PEG-400; sodium hydroxide; for 0.0333333h; microwave irradiation;
Guidance literature:
bromobenzene; With n-butyllithium; In tetrahydrofuran; at -78 ℃; Inert atmosphere;
With zinc(II) chloride; In tetrahydrofuran; at 20 ℃; Inert atmosphere;
C12H13F3O2; With zinc(II) chloride; In toluene; at 50 ℃; for 24h; Inert atmosphere;
DOI:10.1002/anie.201002116
Guidance literature:
With nickel(II) bromide dimethoxyethane; Ir[2-(2,4-difluorophenyl)-5-trifluoromethylpyridine]2(1,10-phenantroline)PF6; Bathocuproine; diisopropylamine; magnesium bromide; In N,N-dimethyl-formamide; at 20 ℃; for 24h; regioselective reaction; Inert atmosphere; Glovebox; Sealed tube; Irradiation;
DOI:10.1021/acs.orglett.8b00413
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