135765-81-0

Basic information

• Product Name: (E)-ethyl 2-hydroxyimino-2-phenylacetate
• Synonyms: (E)-ethyl 2-hydroxyimino-2-phenylacetate
• CAS NO: 135765-81-0
• Molecular Weight: 193.202
• Mol File: 135765-81-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (E)-ethyl 2-hydroxyimino-2-phenylacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-ethyl 2-hydroxyimino-2-phenylacetate(135765-81-0)
• EPA Substance Registry System: (E)-ethyl 2-hydroxyimino-2-phenylacetate(135765-81-0)

Safety Data

• Hazardous Substances Data: 135765-81-0(Hazardous Substances Data)

Upstream product

• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 626-35-7 nitroacetic acid ethyl ester 
• 71-43-2 benzene 
• 83-13-6 diethyl 2-phenylmalonate 
• 101-97-3 Ethyl 2-phenylethanoate 
• 23502-06-9 α-(Acetoximino)-phenylessigsaeure-ethylester 
• 2882-19-1 ethyl 2-phenyl-2-bromoacetate 

Downstream Products

• 32971-23-6 2-hydroxyimino-2-phenyl-acetohydroxamic acid 
• 38114-34-0 2-hydroxyimino-2-phenylacetic acid methyl ester 
• 25327-37-1 2-oximino-2-phenyl-acetamide 
• 23502-06-9 α-(Acetoximino)-phenylessigsaeure-ethylester 
• 77426-82-5 2-(hydroxyimino)-N-methyl-2-phenylacetamide 
• 189570-03-4 4-Ethoxy-3-phenyl-[1,2]oxazin-6-one 
• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 20989-17-7 Phenylglycinol 
• 56613-80-0 D-2-phenylglycinol 
• 20989-17-7 (2S)-2-phenylglycinol 
• 866540-61-6 C₂₂H₂₀NO₃P 
• 14257-84-2 N-acetyl-α-phenylglycine 
• 2835-06-5 phenylglycin 
• 1418119-48-8 ethyl (E)-2-[(2,4-dinitrophenyl)sulfonyloxy]imino-2-phenylacetate 

Relevant articles and documents

Nano-K2CO3: Preparation, characterization and evaluation of reactive activities

A novel base, nano-K2CO3, was easily prepared by ultrafine wet milling. The surface properties and the reactive activities of nano-K2CO3 were characterized. It was found that such a base showed higher basicity than normal K2CO3 and could replace sodium (or potassium) alkoxide to carry out monoalkylation and oximation of active methylene compounds. The nano-K2CO3 could be regenarated and reused 10 times without loss of its reactive activity.

Superacid and thiol-ene reactions for access to psammaplin analogues with HDAC inhibition activities Dedicated to Professor Jean Marie Coustard, a creative chemist

An innovative synthesis of psammaplin-like structure is proposed based on original methodologies using superacid, microwaves, and S-ene chemistry. The new compounds were evaluated as histone deacetylase inhibitors. The results highlight important consider

Hydroxynitrilium ions as intermediates in the reaction of nitroderivatives with aromatics

In acids reaction of ethyl nitroacetate 1 and of a nitroacetophenone 14 with aromatics yields E oximes 2 and 15, respectively, addition occurring on the corresponding hydroxynitrilium ion.