885669-11-4

Basic information

• Product Name: N'-PHENYL-N'-(PROP-2-YL)ACETOHYDRAZIDE
• Synonyms: N'-ISOPROPYL-N'-PHENYLACETOHYDRAZIDE;N'-PHENYL-N'-(PROP-2-YL)ACETOHYDRAZIDE;N'-phenyl-N'-(propan-2-yl)acetohydrazide
• CAS NO: 885669-11-4
• Molecular Formula: C₁₁H₁₆N₂O
• Molecular Weight: 192.26
• Mol File: 885669-11-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N'-PHENYL-N'-(PROP-2-YL)ACETOHYDRAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N'-PHENYL-N'-(PROP-2-YL)ACETOHYDRAZIDE(885669-11-4)
• EPA Substance Registry System: N'-PHENYL-N'-(PROP-2-YL)ACETOHYDRAZIDE(885669-11-4)

Safety Data

• Hazardous Substances Data: 885669-11-4(Hazardous Substances Data)

Upstream product

• 35292-56-9 1-(1-Methylethyl)-1-phenylhydrazine 
• 108-24-7 acetic anhydride 
• 75-26-3 isopropyl bromide 
• 114-83-0 1-acetyl-2-phenylhydrazine 
• 13443-97-5 1-methyl-3-phenyl-2,3-diazaprop-2-en-1-one 
• 1068-55-9 isopropylmagnesium chloride 
• 768-52-5 N-Isopropylaniline 

Downstream Products

• 35292-56-9 1-(1-Methylethyl)-1-phenylhydrazine 

Relevant articles and documents

Synthesis method for intermolecular N-N bonding and corresponding synthesized compound

The invention relates to a synthesis method for intermolecular N-N bonding and a corresponding compound. According to the invention, the direct insertion reaction of N-H bonds by nitrene is completed, and a brand-new N-N coupling reaction method is developed. The reaction uses a nitrene precursor, under the action of a catalyst, an intermolecular direct N-N coupling reaction of the nitrene precursor and an amine compound can be realized, and a tetra-substituted hydrazine compound is constructed in one step.

Novel, efficient and regiospecific alkylation/arylation/heteroarylation of unsymmetrical azo compounds

Excellent regioselectivity is observed in the addition of diverse organometallic nucleophiles to unsymmetrical azo compounds. Primary/secondary/ tertiary alkyl, aryl and heteroaryl substituents were introduced this way in high yields. Georg Thieme Verlag