6828-55-3

Basic information

• Product Name: N-benzoyl-4-chloro-benzohydrazide
• CAS NO: 6828-55-3
• Molecular Formula: C₁₄H₁₁ClN₂O₂
• Molecular Weight: 274.707
• Mol File: 6828-55-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 524°Cat760mmHg
• Flash Point: 270.7°C
• Density: 1.308g/cm³
• CAS DataBase Reference: N-benzoyl-4-chloro-benzohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzoyl-4-chloro-benzohydrazide(6828-55-3)
• EPA Substance Registry System: N-benzoyl-4-chloro-benzohydrazide(6828-55-3)

Safety Data

• Hazardous Substances Data: 6828-55-3(Hazardous Substances Data)

Upstream product

• 613-94-5 benzoic acid hydrazide 
• 74-11-3 para-chlorobenzoic acid 
• 536-40-3 4-chlorobenzoic acid hydrazide 
• 65-85-0 benzoic acid 
• 98-88-4 benzoyl chloride 
• 1126-46-1 Methyl 4-chlorobenzoate 
• 155164-66-2 2-benzoyl-4,5-dichloropyridazin-3(2H)-one 
• 450408-66-9 4,5-dichloro-2-(4-chloro-benzoyl)-2H-pyridazin-3-one 

Downstream Products

• 1156534-46-1 2-(4-chlorophenyl)-5-phenyl-1,3,4-selenadiazole 
• 471910-33-5 3-(4-chlorophenyl)-4-methyl-5-phenyl-4H-1,2,4-triazole 
• 87277-53-0 3-(4-chlorophenyl)-5-phenyl-1H-1,2,4-triazole 
• 87277-51-8 1-methyl-5-(4-chlorophenyl)-3-phenyl-1H-1,2,4-triazole 
• 87277-52-9 3-(4-Chloro-phenyl)-1-methyl-5-phenyl-1H-[1,2,4]triazole 
• 10465-84-6 4-Chlor-azodibenzoyl 
• 106-47-8 4-chloro-aniline 
• 62-53-3 aniline 
• 1874-43-7 2-(4-chlorophenyl)-5-phenyl-1,3,4-oxadiazole 

Relevant articles and documents

One-Pot Catalytic Approach for the Selective Aerobic Synthesis of Imines from Alcohols and Amines Using Efficient Arene Diruthenium(II) Catalysts under Mild Conditions

A green and efficient catalytic approach for the selective synthesis of imines in air at room temperature was achieved with the aid of newly synthesised diruthenium(II) complexes [(η6-p-cymene)2Ru2Cl2(μ-L)] containing substituted 1,2-diacylhydrazine ligands. All the new complexes were fully characterised by analytical and spectroscopic techniques. The solid-state structure of a representative complex was solved by single-crystal X-ray diffraction analysis. The diruthenium(II) complexes also enable the selective aerobic oxidation of alcohols to aldehydes. The catalytic reaction operates in the presence of air as a green and cheap oxidant, and releases water as the only by-product. A plausible mechanism is proposed for the imine formation, which is believed to proceed via an aldehyde intermediate.

17O NMR studies of substituted 1,3,4-oxadiazoles

Three series of substituted 1,3,4-oxadiazoles were studied by 17O NMR spectroscopy. Chemical shifts values were correlated with empirical Hammett parameters as well as calculated bond lengths and chemical shielding values.

Facile synthesis of symmetric and unsymmetric 1,3,4-oxadiazoles using 2-acyl(or aroyl)pyridazin-3-ones

Symmetric and unsymmetric 1,3,4-oxadiazoles were synthesized in situ from hydrazine hydrate and the corresponding 2-acyl-4,5-dichloropyridazin-3-ones as acylating agents in polyphosphoric acid or BF3·OEt2 in excellent yields.