6784-22-1

Basic information

• Product Name: Oxanilonitrile
• CAS NO: 6784-22-1
• Molecular Weight: 146.148
• Mol File: 6784-22-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Oxanilonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: Oxanilonitrile(6784-22-1)
• EPA Substance Registry System: Oxanilonitrile(6784-22-1)

Safety Data

• Hazardous Substances Data: 6784-22-1(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 215436-24-1 2,2-dimethyl-5-(p-tosyloxyimino)-1,3-dioxane-4,6-dione 
• 74-90-8 hydrogen cyanide 
• 103-71-9 phenyl isocyanate 
• 71-43-2 benzene 
• 7719-09-7 thionyl chloride 
• 42366-35-8 hydroxyimino-N-phenylacetamide 
• 7664-93-9 sulfuric acid 
• 6343-76-6 1-cyano-N,N-diphenylformamidine 
• 52744-74-8 2-(hydroxyimino)-3-oxo-N,3-diphenylpropanamide 
• 105-56-6 ethyl 2-cyanoacetate 
• 2352-40-1 2-(hydroxyimino)-3-oxo-N-phenylbutanamide 
• 4955-82-2 1-cyanothioformanilide 
• 58393-33-2 3-Oxo-1,1-dicyanbutyl-cyanformiat 

Downstream Products

• 18629-86-2 2-acetyl-N-phenyl-malonamic acid ethyl ester 
• 74-90-8 hydrogen cyanide 
• 101-99-5 N-carboethoxyaniline 
• 64-10-8 phenyl carbamate 
• 10319-52-5 5-imino-1,3-diphenyl-imidazolidine-2,4-dione 
• 10543-64-3 phenyl-oxalamide 
• 500-72-1 oxanilic acid 
• 125244-74-8 oxanilic acid thioamide 
• 91-56-5 indole-2,3-dione 
• 103-71-9 phenyl isocyanate 
• 102-07-8 bis(diphenyl)urea 
• 621-12-5 1,4-diphenylsemicarbazide 
• 603-54-3 N,N-diphenylurea 
• 7664-41-7 ammonia 

Relevant articles and documents

4,5-Dioxo-imidazolinium Cation Activation of 1-Acyl-1-carbamoyl Oximes: Access to Cyanoformamides Using Dichloroimidazolidinedione

Cyanoformamides are prevalent as versatile building blocks for accessing synthetically useful intermediates and biologically active compounds. The development of a milder, simpler, and more efficient approach to cyanoformamides is nontrivial. Herein, we demonstrate the effectiveness of 4,5-dioxo-imidazolinium cation activation for transforming 1-acyl-1-carbamoyl oximes to cyanoformamides. By making use of the readily available and highly modifiable dichloroimidazolidinediones (DCIDs), this novel method of activation offers reactivity remarkably greater than that of other reported protocols, exhibits a high functional group compatibility with mild conditions, and could be scaled up easily. More than 30 examples are demonstrated with good to excellent yields in short reaction times. This research not only provides a mild and efficient alternative approach to assembling a portfolio of cyanoformamides but also extends the dichloroimidazolidinedione-mediated chemistry to encompass the C-C bond cleavage reaction.

Synthesis method of cyano-formamide compound

The invention discloses a synthesis method of a cyano-formamide compound, and relates to the technical field of chemical synthesis. The cyano-formamide compound shown in the formula III is synthesizedfrom a 1-acyl-1-carbamyl oxime compound shown in the fo

POCl3-mediated reaction of 1-Acyl-1-carbamoyl Oximes: A new entry to cyanoformamides

A facile and efficient one-pot synthesis of cyanoformamides was developed from readily available 1-acyl-1-carbamoyl oximes mediated by phosphoryltrichloride (POCl3) under mild conditions in good to high yields.