4-(2-Phenylbenzoylamino)-benzoylchloride

Base Information

Chemical Name:4-(2-Phenylbenzoylamino)-benzoylchloride
CAS No.:180340-05-0
Molecular Formula:C20H14ClNO2
Molecular Weight:335.79
Hs Code.:
DSSTox Substance ID:DTXSID80466327
Nikkaji Number:J1.645.296C
Wikidata:Q82292866
Mol file:180340-05-0.mol

Synonyms:180340-05-0;4-(2-phenylbenzoylamino)-benzoylchloride;SCHEMBL2571007;DTXSID80466327;PAKGPZHOIVVKMH-UHFFFAOYSA-N;4-(2-phenylbenzoylamino)benzoyl chloride;4-[(Biphenyl-2-carbonyl)-amino]-benzoyl Chloride;4-[(Bi phenyl-2-carbonyl)-amino]-benzoyl chloride;4-[([1,1'-Biphenyl]-2-carbonyl)amino]benzoyl Chloride;4-[([1, 1'-biphenyl]-2-carbonyl)amino]-benzoyl chloride;4-[([1,1'-biphenyl]-2-carbonyl)amino]-benzoyl chloride

Suppliers and Price of 4-(2-Phenylbenzoylamino)-benzoylchloride

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
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price

Total 1 raw suppliers

Chemical Property of 4-(2-Phenylbenzoylamino)-benzoylchloride

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:335.0713064
Heavy Atom Count:24
Complexity:439

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC=CC=C2C(=O)NC3=CC=C(C=C3)C(=O)Cl

Technology Process of 4-(2-Phenylbenzoylamino)-benzoylchloride

There total 5 articles about 4-(2-Phenylbenzoylamino)-benzoylchloride 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:

: 168626-74-2
4-[([1,1'-Biphenyl]-2-carbonyl)amino]benzoic Acid

: 180340-05-0
4-[([1,1'-biphenyl]-2-carbonyl)amino]-benzoyl chloride

Guidance literature:: With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; for 1h;
DOI:10.1248/cpb.46.1566

Reference yield:

: 94-09-7
p-aminoethylbenzoate

: 180340-05-0
4-[([1,1'-biphenyl]-2-carbonyl)amino]-benzoyl chloride

Guidance literature:: Multi-step reaction with 3 steps

1: 8.1 percent / WSC, HOBt / tetrahydrofuran / 240 h / Ambient temperature

2: 86 percent / 1 N NaOH / ethanol / 18 h / Ambient temperature

3: oxalyl chloride, DMF / CH₂Cl₂ / 1 h

With sodium hydroxide; oxalyl dichloride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N,N-dimethyl-formamide; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1248/cpb.46.1566

Reference yield:

: 217495-89-1
ethyl 4-([1,1'-biphenyl]-2-carboxamido)benzoate

: 180340-05-0
4-[([1,1'-biphenyl]-2-carbonyl)amino]-benzoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / 1 N NaOH / ethanol / 18 h / Ambient temperature

2: oxalyl chloride, DMF / CH₂Cl₂ / 1 h

With sodium hydroxide; oxalyl dichloride; N,N-dimethyl-formamide; In ethanol; dichloromethane;
DOI:10.1248/cpb.46.1566