5171-99-3

Basic information

• Product Name: (1-phenylpropan-2-ylidene)hydrazine
• Synonyms: (1-phenylpropan-2-ylidene)hydrazine
• CAS NO: 5171-99-3
• Molecular Weight: 148.208
• Mol File: 5171-99-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1-phenylpropan-2-ylidene)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: (1-phenylpropan-2-ylidene)hydrazine(5171-99-3)
• EPA Substance Registry System: (1-phenylpropan-2-ylidene)hydrazine(5171-99-3)

Safety Data

• Hazardous Substances Data: 5171-99-3(Hazardous Substances Data)

Upstream product

• 10147-11-2 propargyl benzene 
• 103-79-7 1-phenyl-acetone 

Downstream Products

• 55-52-7 pheniprazine 
• 60-15-1 2-amino-1-phenylpropane 
• 16602-89-4 N,N'-bis-(1-methyl-2-phenyl-ethyl)-hydrazine 
• 53001-42-6 (Z)-2-{N'-[1-Methyl-2-phenyl-eth-(E)-ylidene]-hydrazino}-hept-2-en-5-yn-4-one 
• 300-57-2 allylbenzene 
• 766-90-5 cis-1-phenyl-1-propylene 
• 117747-35-0 2-((3-phenylprop-1-en-2-yl)oxy)benzaldehyde 
• 103-79-7 1-phenyl-acetone 
• 3712-58-1 [(1-methyl-2-phenyl-ethyl)-hydrazine-N,N-diyl]-bis-methanesulfonic acid 
• 109000-23-9 1-phenyl-2-iodopropene 
• 58325-18-1 2,2-Difluoro-1-phenylpropane 
• 79462-37-6 dibromo-2,2 phenyl-1 propane 
• 29443-57-0 1-phenyl-2,2-diiodopropane 
• 29443-56-9 2-iodo-3-phenylpropene 

Relevant articles and documents

Exploring the Influence of Phosphine Ligation on the Gold-Catalyzed Hydrohydrazination of Terminal Alkynes at Room Temperature

The synthesis and/or NMR/X-ray characterization of a new series of (L)AuCl complexes is reported, featuring BippyPhos, AdJohnPhos, silyl ether based ligands including OTips-DalPhos, and PAd-DalPhos. These complexes, along with previously reported analogue

Room-temperature hydrohydrazination of terminal alkynes catalyzed by saturated abnormal n-heterocyclic carbene-gold(I) complexes

A number of saturated abnormal N-heterocyclic carbene (NHC) complexes of gold, in combination with KBArF4 as activator, were successfully applied in the chemoselective addition of hydrazine to alkynes. The reaction proceeds even at r

Gold-catalyzed hydroamination of alkynes and allenes with parent hydrazine

A diverse array of nitrogen-containing compounds were formed by the addition of hydrazine to alkynes, diynes, enynes, and allenes in the presence of cationic gold(I) complexes with a cyclic (alkyl)(amino)carbene ligand (see scheme; the X-ray crystal structure of the gold-hydrazine complex is shown). This hydroamination is an ideal initial step for the preparation of acyclic and heterocyclic bulk chemicals. Dipp=2,6-diisopropylphenyl. Copyright