288254-83-1

Basic information

• Product Name: Benzoic acid, 4-(trifluoromethyl)-, 2-benzoylhydrazide
• CAS NO: 288254-83-1
• Molecular Formula: C15H11F3N2O2
• Molecular Weight: 308.26
• Mol File: 288254-83-1.mol

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(trifluoromethyl)-, 2-benzoylhydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(trifluoromethyl)-, 2-benzoylhydrazide(288254-83-1)
• EPA Substance Registry System: Benzoic acid, 4-(trifluoromethyl)-, 2-benzoylhydrazide(288254-83-1)

Safety Data

• Hazardous Substances Data: 288254-83-1(Hazardous Substances Data)

Upstream product

• 2967-66-0 methyl 4-(trifluoromethyl)benzoate 
• 339-59-3 4-(trifluoromethyl)benzoic acid hydrazide 
• 98-88-4 benzoyl chloride 
• 402-43-7 p-trifluoromethylphenyl bromide 
• 613-94-5 benzoic acid hydrazide 
• 455-13-0 4-Iodobenzotrifluoride 
• 329-15-7 4-trifluoromethyl-phenyl acetyl chloride 

Downstream Products

• 471910-35-7 3-(4-trifluoromethylphenyl)-4-methyl-5-phenyl-4H-1,2,4-triazole 
• 89804-59-1 5-phenyl-3-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazole 
• 89804-60-4 1-methyl-5-(4-trifluoromethylphenyl)-3-phenyl-1H-1,2,4-triazole 
• 724434-37-1 2-phenyl-5-[4-(trifluoromethyl)phenyl]-1,3,4-oxadiazole 

Relevant articles and documents

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.

Direct microwave synthesis of N,N′-diacylhydrazines and boc-protected hydrazides by in situ carbonylations under air

Palladium-catalyzed hydrazidocarbonylations of aryl iodides and bromides were performed by controlled microwave irradiation, employing Mo(CO)6 as a convenient CO source. A fluorous phosphine ligand was succesfully used to recycle the catalytic

Regioselectivity in the thermal rearrangement of unsymmetrical 4-methyl-4H-1,2,4-triazoles to 1-methyl-1H-1,2,4-triazoles

The rearrangement of 4-methyl-3,5-diaryl-4H-1,2,4-triazoles to the corresponding 1-methyl-3,5-diaryl-1H-1,2,4-triazoles showed regioselectivity comparable to that observed for the alkylation of 3,5-diaryl-1H-1,2,4-triazoles. This lends support to a proposed mechanism for the rearrangement that involves consecutive nucleophilic displacements steps.