1888389-19-2

Basic information

• Product Name: (2E)-N-(3-FLUOROPHENYL)-2-(HYDROXYIMINO)ACETAMIDE
• Synonyms: N-(3-fluorophenyl)-2-(N-hydroxyimino)acetamide;(2E)-N-(3-FLUOROPHENYL)-2-(HYDROXYIMINO)ACETAMIDE
• CAS NO: 1888389-19-2
• Molecular Formula: C8H7FN2O2
• Molecular Weight: 182.15
• Mol File: 1888389-19-2.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2E)-N-(3-FLUOROPHENYL)-2-(HYDROXYIMINO)ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-N-(3-FLUOROPHENYL)-2-(HYDROXYIMINO)ACETAMIDE(1888389-19-2)
• EPA Substance Registry System: (2E)-N-(3-FLUOROPHENYL)-2-(HYDROXYIMINO)ACETAMIDE(1888389-19-2)

Safety Data

• Hazardous Substances Data: 1888389-19-2(Hazardous Substances Data)

Upstream product

• 372-19-0 meta-fluoroaniline 
• 302-17-0 chloral hydrate 
• 75-87-6 chloral 

Downstream Products

• 324-03-8 6-fluoroisatin 
• 2341-25-5 2-(6-fluoro-1H-indol-3-yl)acetonitrile 
• 915923-73-8 7-fluoro-2-methyl-quinoline-4-carboxylic acid 
• 1020958-90-0 2-(6-fluoro-2,3-dioxoindolin-1-yl)-N-phenylacetamide 
• 2713-68-0 2-(carboxymethyl-amino)-4-fluoro-benzoic acid 
• 346-34-9 4-fluoro-1H-indole-2,3-dione 

Relevant articles and documents

A NOVEL PROCESS FOR THE PREPARATION OF TRYPTAMINES AND DERIVATIVES THEREOF

The present invention relates to a novel process for the preparation of tryptamine, its substituted derivatives and intermediates for the preparation of them.

NITROGENATED HETEROCYCLIC COMPOUND AND AGRICULTURAL OR HORTICULTURAL FUNGICIDE

An agricultural or horticultural fungicide contains as an active ingredient thereof at least one compound selected from the group consisting of nitrogenated heterocyclic compounds represented by formula (I) (wherein, R represents a group represented by CR

Novel synthesis of 4-or 6-substituted indirubin derivatives

A simple and convenient route for synthesis of a series of 4-or 6-substituted indirubin derivatives by oxidation and subsequent condensation of indoxyl and isatin is described. Acidic reaction conditions are crucial to the condensation of 4-substituted derivatives, whereas for the condensation of 6-substituted derivatives, both acidic and basic conditions work well. Copyright Taylor & Francis Group, LLC.