93515-65-2

Basic information

• Product Name: p-toluoyl isoselenocyanate
• Synonyms: p-toluoyl isoselenocyanate
• CAS NO: 93515-65-2
• Molecular Weight: 224.121
• Mol File: 93515-65-2.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: p-toluoyl isoselenocyanate(CAS DataBase Reference)
• NIST Chemistry Reference: p-toluoyl isoselenocyanate(93515-65-2)
• EPA Substance Registry System: p-toluoyl isoselenocyanate(93515-65-2)

Safety Data

• Hazardous Substances Data: 93515-65-2(Hazardous Substances Data)

Upstream product

• 3425-46-5 potassium selenocyanate 
• 874-60-2 4-methyl-benzoyl chloride 

Downstream Products

• 905996-57-8 1-phenyl-4-p-toluoylselenosemicarbazide 
• 905996-51-2 2-phenyl-5-p-tolyl-1,2-dihydro-3H-1,2,4-triazole-3-selone 

Relevant articles and documents

Synthesis of 4-aryl-1,3,4a-triazaphenanthrene-2-selones via three-component condensation of quinolin-2-amine, potassium selenocyanate and an acyl chloride

A three-component reaction between quinolin-2-amine, potassium selenocyanate and variously substituted benzoyl chlorides in acetone at room temperature provided a simple and efficient one-pot route for the synthesis of six 4-aryl-1,3,4a-triazaphenanthrene

An Efficient Synthesis of Novel 1,3,5-Triazine-2-selenones from Acyl Isoselenocyanates and 2-Aminobenzimidazole

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Synthesis of 4-aryl-7-methoxy-9-thia-[1,3,4a]triazafluorene-2-selones via a three-component condensation of 6-methoxybenzothiazol-2-ylamine, potassium selenocyanate and an acyl chloride

A simple, one-pot synthesis of six 4-aryl-7-methoxy-9-thia-[1,3,4a]triazafluorene-2-selones has been achieved in moderate to good yields via a three-component condensation of 6-methoxybenzothiazol-2-ylamine, potassium selenocyanate and variously substitut

Synthesis of 2-aryl-7-methyl-4-selenoxo-4H-pyrano[3,4-e][1,3]oxazin-5-one via a three-component condensation

The reaction between 4-hydroxy-6-methyl-2H-pyran-2-one and aroyl chlorides with potassium selenocyanate in the presence of catalytic amounts of N-methylimidazole under solvent-free conditions provided a simple and efficient one-pot route for the synthesis