80055-47-6

Basic information

• Product Name: 4-nitro-benzaldehyde-((E)-O-acetyl oxime )
• Synonyms: 4-nitro-benzaldehyde-((E)-O-acetyl oxime )
• CAS NO: 80055-47-6
• Molecular Weight: 208.174
• Mol File: 80055-47-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-nitro-benzaldehyde-((E)-O-acetyl oxime )(CAS DataBase Reference)
• NIST Chemistry Reference: 4-nitro-benzaldehyde-((E)-O-acetyl oxime )(80055-47-6)
• EPA Substance Registry System: 4-nitro-benzaldehyde-((E)-O-acetyl oxime )(80055-47-6)

Safety Data

• Hazardous Substances Data: 80055-47-6(Hazardous Substances Data)

Upstream product

• 1129-37-9 4-nitrobenzaldoxime 
• 108-24-7 acetic anhydride 
• 830-03-5 4-nitrophenol acetate 
• 1129-37-9 4-nitrobenzaldehyde oxime 
• 463-51-4 Ketene 
• 60-29-7 diethyl ether 

Downstream Products

• 1129-37-9 4-nitrobenzaldehyde oxime 
• 62-23-7 4-nitro-benzoic acid 
• 619-72-7 4-nitrobenzonitrile 
• 1129-37-9 4-nitrobenzaldoxime 

Relevant articles and documents

EFFETS MICELLAIRES SUR LA BASICITE ET LA REACTIVITE DE NUCLEOPHILES α AROMATIQUES

The oximation of p-nitrophenylacetate by benzaldoximates in aqueous solution is catalyzed by CTAB micelles.The catalysis is more effective when the base strength of the oximate decreases; the reactivity of benzaldoximates is not dependent on their basicity.Our data may be interpreted in terms of orbital-controlled reactions, with interactions between both the n and ? occupied orbitals of the oximates and the LUMO of the acetate.