5455-22-1

Basic information

• Product Name: Benzoic acid 1-phenyl-2-benzoyl hydrazide
• Synonyms: 1,2-Dibenzoyl-1-phenylhydrazine;Benzoic acid 1-phenyl-2-benzoyl hydrazide;N'-Benzoyl-N-phenylbenzohydrazide
• CAS NO: 5455-22-1
• Molecular Formula: C₂₀H₁₆N₂O₂
• Molecular Weight: 316.35
• Mol File: 5455-22-1.mol

Chemical Properties

• Appearance: /
• Density: 1.24 g/cm³
• CAS DataBase Reference: Benzoic acid 1-phenyl-2-benzoyl hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid 1-phenyl-2-benzoyl hydrazide(5455-22-1)
• EPA Substance Registry System: Benzoic acid 1-phenyl-2-benzoyl hydrazide(5455-22-1)

Safety Data

• Hazardous Substances Data: 5455-22-1(Hazardous Substances Data)

Usage

Uses

Used in Organic and Pharmaceutical Synthesis:
Benzoic acid 1-phenyl-2-benzoyl hydrazide is used as a reagent in organic and pharmaceutical synthesis, particularly in the preparation of heterocyclic compounds and pharmaceutical intermediates. Its unique structure and properties make it a valuable component in the development of new drugs and chemical compounds.
Used in Dye and Pigment Production:
Benzoic acid 1-phenyl-2-benzoyl hydrazide is also used as a chemical intermediate in the production of dyes and pigments. Its ability to form stable complexes with other molecules contributes to the color and stability of these products.
Used in Pharmaceutical Research:
Benzoic acid 1-phenyl-2-benzoyl hydrazide has been studied for its potential pharmacological properties, including its anti-inflammatory and analgesic effects. Its ability to modulate various biological pathways and exhibit therapeutic effects makes it a promising candidate for further research and development in the pharmaceutical industry.

Upstream product

• 98-88-4 benzoyl chloride 
• 59-88-1 phenylhydrazine hydrochloride 
• 59105-56-5 phenyl-hydrazine; sodium-compound 
• 583-11-9 N-(1-phenylethylidene)phenylhydrazine 
• 100-63-0 phenylhydrazine 
• 71-43-2 benzene 
• 579-45-3 N-benzoyl-N-phenylhydrazine 
• 60-29-7 diethyl ether 
• 935-07-9 acetaldehyde phenylhydrazone 
• 14353-52-7 phenyldithiocarbazic acid 
• 532-96-7 N-benzoyl-N'-phenylhydrazine 
• 959-31-9 1,2-dibenzoyldiazene 
• 698-16-8 benzohydroximoyl chloride 
• 952-53-4 1,3-diphenyl-2,3-diazaprop-2-en-1-one 

Downstream Products

• 13370-06-4 1,5-diphenyl-4-pyrazolin-3-one 
• 89499-55-8 1-acetyl-2-phenyl-1,2-dibenzoylhydrazine 
• 1043-46-5 1,3,5-triphenyl-1,2,4-triazole 
• 102311-46-6 N,N'-dibenzoyl-N-methyl-N'-phenyl-hydrazine 
• 93-98-1 N-phenyl benzoyl amide 
• 100-52-7 benzaldehyde 
• 65-85-0 benzoic acid 
• 532-96-7 N-benzoyl-N'-phenylhydrazine 
• 100-63-0 phenylhydrazine 
• 857796-55-5 benzoic acid-[N'-(3-oxo-3-phenyl-propenyl)-N'-phenyl-hydrazide] 
• 4406-66-0 phenylazomethane 
• 622-36-6 1-methyl-2-phenylhydrazine 

Relevant articles and documents

1,2-Diacyl-1-arylhydrazines: II. Molecular and Crystal Structure of 1,2-Dibenzoyl-1-phenylhydrazines and 2-Acetyl-1-(4-nitrophenyl)-1-salicyloylhydrazines

Molecules of 1,2-dibenzoyl-1-phenyl- and 2-acetyl-1-(4-nitrophenyl)-1-salicyloylhydrazines are nonplanar, the unshared electron pairs of the nitrogen atoms in them are orthogonal to each other, and the torsion angle about the amide bonds depends on the nature of substituents at the nitrogen atoms. The molecules in crystal pack in infinite chains formed by intermolecular hydrogen bonds.

The Reaction of 1-(N-Phenacylidene)amino-1,2,3-triazoles with Diphenylnitrilimine

Diphenylnitrilimine reacts with 1-(N-phenacylidene)amino-1,2,3-triazoles 1 to give mainly 1,2,4- and 2H-1,2,3-triazoles 2 and 3.CNDO/2 calculations were made on the compounds 1 and the cycloaddition was also examined on the basis of the interacting fronti

RECYCLIZATION REACTIONS. 26. RECYCLIZATION OF HETEROARENIUM SALTS BY ACTION OF ACID ANHYDRIDE IN THE PRESENCE OF BASE

When oxazolium, 1,3,4-thia- and -selenodiazolium, or pyrylium salts react with acid anhydride in the presence of base, they are recyclized to pyrrole, pyrazole, and benzene derivatives, respectively.The typical features of recyclization involving anhydride in a number of five-membered systems are discussed.

Thermal Decomposition of Liquid α-Nitrotoluene

Liquid α-nitrotoluene decomposes on heating into benzonitrile, benzaldehyde, benzaldehyde oxime, oxides of nitrogen, and water.Prolonged heating (over 2 h) at 125 deg C leads to N,N'-dibenzoyl-N-phenylhydrazine, α-nitrostilbene, 3,4,5-triphenylisoxazole, 1,3,5-triphenyl-1,2,4-triazole, 3,5-diphenyl-1,2,4-oxadiazole, benzamide, benzylideneaniline, benzanilide, and trans-stilbene.The product distribution depends on the temperature and duration of heating.