93885-67-7

Usage

Usage

Building block in organic synthesis

Applications

Production of pharmaceuticals, agrochemicals, and dyes

Physical State at Room Temperature

Pale yellow solid

Melting Point

66-68°C

Boiling Point

274-275°C

Safety Precautions

Harmful if in contact with skin or inhaled

Upstream product

• 2826-25-7 2-(4-methylbenzylidene)malononitrile 
• 151-50-8 potassium cyanide 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 112212-03-0 5-amino-3,4-dicyano-2,2-dimethyl-3-(4-tolyl)-2,3-dihydro-oxole 
• 7634-91-5 2-(4-methylphenyl)-1,1,2-tricyanoethylene 
• 112212-08-5 3,4-dicyano-2,2-dimethyl-5-oxo-3-(4-tolyl)oxolane 

Relevant academic research and scientific papers

Sizeable red-shift of absorption and fluorescence of subporphyrazine induced by peripheral push and pull substitution

Peripheral substitution with electron-donating (push) and electron-withdrawing (pull) substituents caused a sizeable red-shift of the Q band absorption and fluorescence of subporphyrazine, and the red-shift was controlled by the push substituents. Control

Synthesis and Trasformations of 5-Amino-2,3-dihydro-oxoles

Treatment of α-cyanocinnamonitriles 1 with hydrogen cyanide in acetone results in the formation of 5-amino-2,3-dihydro-oxoles 3.Tricyanoethanes 2 can be obtained as intermediate compounds in a two-step process leading to the same dihydro-oxoles.Acid hydro