(4-Chlorophenyl)(4-phenoxyphenyl)methanone

Base Information

• Chemical Name: (4-Chlorophenyl)(4-phenoxyphenyl)methanone
• CAS No.: 28315-73-3
• Molecular Formula: C19H13 Cl O2
• Molecular Weight: 308.764
• NSC Number: 123097
• DSSTox Substance ID: DTXSID90298434
• Wikidata: Q82040243
• Mol file: 28315-73-3.mol

Synonyms:(4-chlorophenyl)(4-phenoxyphenyl)methanone;28315-73-3;NSC 123097;NSC123097;SCHEMBL6032445;DTXSID90298434;NSC-123097;(4-Chloro-phenyl)-(4-phenoxy-phenyl)-methanone

Chemical Property of (4-Chlorophenyl)(4-phenoxyphenyl)methanone

Chemical Property:

• Vapor Pressure: 3.86E-08mmHg at 25°C
• Boiling Point: 445.7°Cat760mmHg
• Flash Point: 172.2°C
• Density: 1.234g/cm³
• XLogP3: 5.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 308.0604073
• Heavy Atom Count: 22
• Complexity: 348

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)OC2=CC=C(C=C2)C(=O)C3=CC=C(C=C3)Cl

Technology Process of (4-Chlorophenyl)(4-phenoxyphenyl)methanone

There total 2 articles about (4-Chlorophenyl)(4-phenoxyphenyl)methanone 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:

Reference yield: 74.0%

4-phenoxyphenylboronic acid (51067-38-0) + para-chlorobenzoic acid (74-11-3) → 4-Chlor-4'-phenoxy-benzophenon (28315-73-3)

Guidance literature:

With potassium carbonate; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; palladium dichloride; In acetone; at 20 ℃; for 2h;

DOI:10.1016/j.tetlet.2017.01.064

Reference yield:

→ 4-Chlor-4'-phenoxy-benzophenon (28315-73-3)

Guidance literature:

4-Chlor-4'-nitrobenzophenon, Na-phenolat;

Reference yield: 76.0%

4-Chlor-4'-phenoxy-benzophenon (28315-73-3) + chloroacetonitrile (107-14-2) → 3-(4-chlorophenyl)-3-(4-phenoxyphenyl)oxirane-2-carbonitrile (1052176-01-8)

Guidance literature:

With sodium hydroxide; In tetrahydrofuran; at 20 - 30 ℃; for 0.75h;

upstream raw materials:

4-phenoxyphenylboronic acid

para-chlorobenzoic acid

Downstream raw materials:

3-(4-chlorophenyl)-3-(4-phenoxyphenyl)oxirane-2-carbonitrile

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