Benzenecarbohydrazonic acid, N-phenyl-, phenyl ester

Base Information

• Chemical Name: Benzenecarbohydrazonic acid, N-phenyl-, phenyl ester
• CAS No.: 33491-26-8
• Molecular Formula: C₁₉H₁₆N₂O
• Molecular Weight: 288.349
• NSC Number: 240901

Synonyms:33491-26-8;Benzenecarbohydrazonic acid, N-phenyl-, phenyl ester;POUBLLASFVPRSF-VZCXRCSSSA-N;NSC240901;NSC-240901;Phenyl N-phenylbenzenecarbohydrazonoate #;Benzenecarboximidic acid, N-phenylamino-, phenyl ester

Chemical Property of Benzenecarbohydrazonic acid, N-phenyl-, phenyl ester

Chemical Property:

• Vapor Pressure: 2.97E-07mmHg at 25°C
• Boiling Point: 419.7°Cat760mmHg
• Flash Point: 207.6°C
• Density: 1.07g/cm³
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 288.126263138
• Heavy Atom Count: 22
• Complexity: 337

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)C(=NNC2=CC=CC=C2)OC3=CC=CC=C3
• Isomeric SMILES: C1=CC=C(C=C1)/C(=N/NC2=CC=CC=C2)/OC3=CC=CC=C3

Technology Process of Benzenecarbohydrazonic acid, N-phenyl-, phenyl ester

There total 3 articles about Benzenecarbohydrazonic acid, N-phenyl-, phenyl ester 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: 30.0%

2,5-diphenyl-2H-tetrazole (18039-45-7) + phenol (108-95-2,27073-41-2) → Phenyl-N-phenyl-benzohydrazonat (33491-26-8) + 1,3,5-triphenyl-1,2,4-triazole (1043-46-5) + 2,4,5-triphenyl-2H-[1,2,3]triazole (27653-10-7) + 1,3,4,6-tetraphenyl-1,4-dihydro-1,2,4,5-tetrazine (17355-78-1)

Guidance literature:

In ethanol; Irradiation;

Reference yield:

N-phenylbenzohydrazonoyl chloride (15424-14-3) + phenol (108-95-2,27073-41-2) → Phenyl-N-phenyl-benzohydrazonat (33491-26-8)

Guidance literature:

With triethylamine; Multistep reaction;

Reference yield:

→ Phenyl-N-phenyl-benzohydrazonat (33491-26-8)

Guidance literature:

N-Phenyl-benzoylhydrazonylchlorid, Phenol;

upstream raw materials:

2,5-diphenyl-2H-tetrazole

phenol

N-phenylbenzohydrazonoyl chloride

Downstream raw materials:

N',N'-diphenylbenzohydrazide

N'-phenyl-N'-p-tolylbenzohydrazide

N'-phenyl-N'-m-tolylbenzohydrazide

Benzoic acid N'-phenyl-N'-o-tolyl-hydrazide

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