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phenanthren-9-ylacetyl chloride

Base Information Edit
  • Chemical Name:phenanthren-9-ylacetyl chloride
  • CAS No.:98677-87-3
  • Molecular Formula:C16H11ClO
  • Molecular Weight:254.716
  • Hs Code.:
  • Mol file:98677-87-3.mol
phenanthren-9-ylacetyl chloride

Synonyms:

Suppliers and Price of phenanthren-9-ylacetyl chloride
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of phenanthren-9-ylacetyl chloride Edit
Chemical Property:
  • Vapor Pressure:1.12E-07mmHg at 25°C 
  • Boiling Point:432.4°C at 760 mmHg 
  • Flash Point:213.5°C 
  • Density:1.28g/cm3 
Purity/Quality:
Safty Information:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of phenanthren-9-ylacetyl chloride

There total 5 articles about phenanthren-9-ylacetyl 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 thionyl chloride; for 0.166667h; Heating;
DOI:10.1246/bcsj.56.3118
Guidance literature:
Multi-step reaction with 4 steps
1: 92 percent / N-bromosuccinimide (NBS), benzoyl peroxide / CCl4 / 1 h / Heating
2: 89 percent / ethanol; H2O / 3 h / Heating
3: 93 percent / ethanol. KOH / 20 h / Heating
4: (COCl)2 / CH2Cl2 / 3 h / Ambient temperature
With potassium hydroxide; N-Bromosuccinimide; Perbenzoic acid; oxalyl dichloride; In tetrachloromethane; ethanol; dichloromethane; water;
DOI:10.1021/jo00223a046
Guidance literature:
Multi-step reaction with 2 steps
1: 93 percent / ethanol. KOH / 20 h / Heating
2: (COCl)2 / CH2Cl2 / 3 h / Ambient temperature
With potassium hydroxide; oxalyl dichloride; In dichloromethane;
DOI:10.1021/jo00223a046
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