N'-(4-nitrophenyl)benzohydrazide

Base Information

• Chemical Name: N'-(4-nitrophenyl)benzohydrazide
• CAS No.: 1088-95-5
• Molecular Formula: C13H11N3O3
• Molecular Weight: 257.249
• Hs Code.: 2928000090
• UNII: Z7GGX9CG88
• ChEMBL ID: CHEMBL4059637
• DSSTox Substance ID: DTXSID90148748
• Nikkaji Number: J83.476I
• NSC Number: 56923
• Wikidata: Q83014353
• Mol file: 1088-95-5.mol

Synonyms:N'-(4-nitrophenyl)benzohydrazide;1088-95-5;benzoic acid 2-(p-nitrophenyl)hydrazide;BENZOIC ACID, 2-(p-NITROPHENYL)HYDRAZIDE;NSC-56923;1-Benzoyl-2-(4-nitrophenyl)hydrazine;NSC 56923;BRN 0751540;NSC56923;NCIOpen2_002367;Z7GGX9CG88;3-15-00-00375 (Beilstein Handbook Reference);CHEMBL4059637;SCHEMBL11135287;DTXSID90148748;JJMHIEVGMFNTRR-UHFFFAOYSA-N;N'-(4-nitrophenyl)-benzohydrazide;MFCD00425013;AKOS001644234

Chemical Property of N'-(4-nitrophenyl)benzohydrazide

Chemical Property:

• Vapor Pressure: 2.02E-06mmHg at 25°C
• Melting Point: 193-194 °C(Solv: ethanol (64-17-5))
• Refractive Index: 1.674
• Boiling Point: 394.2 °C at 760 mmHg
• PKA: 11.39±0.23(Predicted)
• Flash Point: 192.2 °C
• PSA: 86.95000
• Density: 1.361 g/cm³
• LogP: 3.33880
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 257.08004122
• Heavy Atom Count: 19
• Complexity: 316

Purity/Quality:

97% ^*data from raw suppliers

N'-(4-Nitrophenyl)benzohydrazide 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=O)NNC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of N'-(4-nitrophenyl)benzohydrazide

There total 14 articles about N'-(4-nitrophenyl)benzohydrazide 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: 85.0%

4a-Morpholin-4-yl-1-(4-nitro-phenyl)-3-phenyl-1,4a,5,6,7,7a-hexahydro-cyclopenta[1,3,4]oxadiazine (106690-01-1) → Benzoic acid N'-(4-nitro-phenyl)-N'-(2-oxo-cyclopentyl)-hydrazide + 1-benzoyl-2-(p-nitrophenyl)hydrazine (1088-95-5)

Guidance literature:

With hydrogenchloride; In acetone; Ambient temperature;

Reference yield: 85.0%

1-(4-Nitro-phenyl)-3-phenyl-4a-piperidin-1-yl-1,4a,5,6,7,7a-hexahydro-cyclopenta[1,3,4]oxadiazine → benzamide (55-21-0,27208-38-4) + 2-p-nitrophenylamino-2-cyclopenten-1-one + Benzoic acid N'-(4-nitro-phenyl)-N'-(2-oxo-cyclopentyl)-hydrazide + 1-benzoyl-2-(p-nitrophenyl)hydrazine (1088-95-5)

Guidance literature:

With hydrogenchloride; In acetone; Ambient temperature;

Reference yield: 83.0%

N-benzoyl-N'-(4-nitrophenyl)diazene (13443-96-4) → 1-benzoyl-2-(p-nitrophenyl)hydrazine (1088-95-5)

Guidance literature:

With phenylhydrazine; In diethyl ether; at 20 ℃;

upstream raw materials:

N-(4-nitro-phenyl)-N-nitroso-benzamidrazone

benzoic acid anhydride

4-nitrophenylhydrazone

1-pyrrolidinocyclopent-1-ene

Downstream raw materials:

benzoic acid-[N'-(4-nitro-phenyl)-N'-phenyl-hydrazide]

N',N'-bis(4-nitrophenyl)benzohydrazide

N-benzoyl-N'-(4-nitrophenyl)diazene

N-(p-nitrophenyl)benzohydrazonoyl chloride