88534-53-6

Usage

Chemical compound

2-Propenal, 3-chloro-3-(4-chlorophenyl)-, oxime

Derivative of

3-chloro-3-(4-chlorophenyl)-2-propenal

Uses

Chemical intermediate in synthesis of various compounds, manufacturing of pharmaceuticals, pesticides, and other organic synthesis processes

Physical properties

Pale yellow solid, stable under normal temperatures and pressures

Safety precautions

Should be handled with care to avoid skin and eye irritation

Environmental considerations

Should be used and disposed of responsibly to minimize environmental impact

Upstream product

• 7089-20-5 [3-chloro-3-(4-chloro-phenyl)-allylidene]-dimethyl-ammonium; perchlorate 
• 14063-77-5 3‐chloro‐3‐(4‐chlorophenyl)acrylaldehyde 

Downstream Products

• 78583-86-5 (E)-3-Chloro-3-(4-chloro-phenyl)-acrylonitrile 

Relevant academic research and scientific papers

Synthesis of a novel series of thieno[3,2-d]pyrimidin-4-(3H)-ones

2-Aminothieno[3,2-d]pyrimidin-4-ones were synthesized in one step by condensation of 3-amino(benzo)thiophene car-boxylate with chloroformamidine hydrochloride. Georg Thieme Verlag Stuttgart.

Synthesis of selenophene analogues of the tacrine series: Comparison of classical route and microwave irradiation

New 3-amino-2-selenophenecarbonitriles condensed with cyclanones to afford, in one step, analogues of Tacrine. A comparison between classical heating and microwave irradiation for the Friedlaender condensation is presented. Georg Thieme Verlag Stuttgart.

A Simple Synthesis of β-Chlorocinnamonitriles by a Modified Vilsmeier-Haack-Arnold-Reaction

A simple one-pot synthesis of β-chloro-cinnamonitriles 2 can be achieved by treating acetyl arenes 1 first with formamide chlorides and subsequently with hydroxyl amine hydrochloride.The formamide chlorides used are conveniently prepared from an excess of