3,5-diphenylbenzoic Acid

Base Information

• Chemical Name: 3,5-diphenylbenzoic Acid
• CAS No.: 99710-75-5
• Molecular Formula: C19H14O2
• Molecular Weight: 274.319
• European Community (EC) Number: 635-589-9
• Nikkaji Number: J948.809J
• Mol file: 99710-75-5.mol

Synonyms:3,5-diphenylbenzoic Acid;3,5-bisphenylbenzoic acid;SCHEMBL4266117;KKNFLGHYWGUFHY-UHFFFAOYSA-N;AKOS024339751;1,1':3',1''-terphenyl-5'-carboxylic acid

Chemical Property of 3,5-diphenylbenzoic Acid

Chemical Property:

• XLogP3: 4.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 274.099379685
• Heavy Atom Count: 21
• Complexity: 314

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC(=CC(=C2)C(=O)O)C3=CC=CC=C3

Technology Process of 3,5-diphenylbenzoic Acid

There total 1 articles about 3,5-diphenylbenzoic Acid 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: 96.6%

3,5-diiodobenzoic acid (19094-48-5) + phenyltin trichloride (1124-19-2) → [1,1′:3′,1″-terphenyl]-5′-carboxylic acid (99710-75-5)

Guidance literature:

With potassium hydroxide; at 40 ℃; for 24h;

DOI:10.1039/c2cy20636f

Reference yield: 28.0%

[1,1′:3′,1″-terphenyl]-5′-carboxylic acid (99710-75-5) + silicon(IV) phthalocyanine dichloride (19333-10-9) → C70H42N8O4Si

Guidance literature:

In diethylene glycol dimethyl ether; at 160 ℃; for 20h;

DOI:10.1016/j.tet.2006.07.046

Reference yield:

[1,1′:3′,1″-terphenyl]-5′-carboxylic acid (99710-75-5) → benzene-1,3,5-tricarboxylic acid (554-95-0)

Guidance literature:

With chromium(III) oxide; sulfuric acid;

upstream raw materials:

3,5-diiodobenzoic acid

phenyltin trichloride

Downstream raw materials:

benzene-1,3,5-tricarboxylic acid

benzoic acid