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2-(2-Phenylethyl)benzoyl chloride

Base Information Edit
  • Chemical Name:2-(2-Phenylethyl)benzoyl chloride
  • CAS No.:36795-27-4
  • Molecular Formula:C15H13ClO
  • Molecular Weight:244.721
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00565205
  • Nikkaji Number:J403.606I
  • Wikidata:Q82450173
  • Mol file:36795-27-4.mol
2-(2-Phenylethyl)benzoyl chloride

Synonyms:2-(2-Phenylethyl)benzoyl chloride;36795-27-4;SCHEMBL7291408;DTXSID00565205;2-bibenzylcarboxylic acid chloride;RNEXBGSRDTZVHE-UHFFFAOYSA-N

Suppliers and Price of 2-(2-Phenylethyl)benzoyl chloride
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
  • Labseeker
  • BENZOYLCHLORIDE,2-(2-PHENYLETHYL)- 95
  • 25g
  • $ 2750.00
  • Labseeker
  • BENZOYLCHLORIDE,2-(2-PHENYLETHYL)- 95
  • 5g
  • $ 1333.00
  • American Custom Chemicals Corporation
  • 2-(2-PHENYLETHYL)BENZOYL CHLORIDE 95.00%
  • 5MG
  • $ 496.96
Total 1 raw suppliers
Chemical Property of 2-(2-Phenylethyl)benzoyl chloride Edit
Chemical Property:
  • PSA:17.07000 
  • LogP:3.85080 
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:4
  • Exact Mass:244.0654927
  • Heavy Atom Count:17
  • Complexity:245
Purity/Quality:

BENZOYLCHLORIDE,2-(2-PHENYLETHYL)- 95 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CCC2=CC=CC=C2C(=O)Cl
Technology Process of 2-(2-Phenylethyl)benzoyl chloride

There total 10 articles about 2-(2-Phenylethyl)benzoyl 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:
Multi-step reaction with 3 steps
1: H2 / 5percent Pd/C / ethanol; ethyl acetate / 0.67 h / 20 °C / 1875.19 Torr
2: aq. NaOH / methanol / 15 h / 20 °C
3: oxalyl chloride; DMF / CH2Cl2 / 1 h / 20 °C
With sodium hydroxide; oxalyl dichloride; hydrogen; N,N-dimethyl-formamide; 5percent Pd/C; In methanol; ethanol; dichloromethane; ethyl acetate;
DOI:10.1021/jm0002073
Guidance literature:
Multi-step reaction with 4 steps
1.1: KOt-Bu / tetrahydrofuran / 1 h / 80 °C
1.2: tetrahydrofuran / 0.5 h / 80 °C
2.1: H2 / 5percent Pd/C / ethanol; ethyl acetate / 0.67 h / 20 °C / 1875.19 Torr
3.1: aq. NaOH / methanol / 15 h / 20 °C
4.1: oxalyl chloride; DMF / CH2Cl2 / 1 h / 20 °C
With sodium hydroxide; oxalyl dichloride; potassium tert-butylate; hydrogen; N,N-dimethyl-formamide; 5percent Pd/C; In tetrahydrofuran; methanol; ethanol; dichloromethane; ethyl acetate;
DOI:10.1021/jm0002073
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