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3,3-Diphenylacryloyl chloride

Base Information
  • Chemical Name:3,3-Diphenylacryloyl chloride
  • CAS No.:4456-79-5
  • Molecular Formula:C15H11ClO
  • Molecular Weight:242.705
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00460221
  • Nikkaji Number:J2.315.779I
3,3-Diphenylacryloyl chloride

Synonyms:3,3-diphenylacryloyl chloride;4456-79-5;3,3-diphenyl-acryloyl chloride;SCHEMBL4398750;DTXSID00460221;GAVZPHQMAKWSMG-UHFFFAOYSA-N;1-chloro-3,3-diphenyl-2-propen-1-one

Suppliers and Price of 3,3-Diphenylacryloyl chloride
Supply Marketing:
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 1 raw suppliers
Chemical Property of 3,3-Diphenylacryloyl chloride
Chemical Property:
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:242.0498427
  • Heavy Atom Count:17
  • Complexity:263
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=CC(=O)Cl)C2=CC=CC=C2
Technology Process of 3,3-Diphenylacryloyl chloride

There total 9 articles about 3,3-Diphenylacryloyl 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:
Guidance literature:
With oxalyl dichloride; N,N-dimethyl-formamide;
DOI:10.1021/jo00798a044
Guidance literature:
Multi-step reaction with 2 steps
1: 3M methanolic KOH / 1 h / Heating
2: (COCl2)2 / toluene / 3 h / Heating
With potassium hydroxide; (COCl2)2; In toluene;
DOI:10.1016/0040-4020(96)00581-9
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / Cooling with ice
1.2: 20 °C
2.1: sodium hydroxide / Reflux
3.1: thionyl chloride / chloroform / 12 h / 20 °C
With thionyl chloride; sodium hydride; sodium hydroxide; In tetrahydrofuran; chloroform; mineral oil;
DOI:10.3998/ark.5550190.0012.230
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