1129-36-8

Basic information

• Product Name: Cyanic acid, 4-acetylphenyl ester (9CI)
• Synonyms: Cyanic acid, 4-acetylphenyl ester (9CI)
• CAS NO: 1129-36-8
• Molecular Formula: C₉H₇NO₂
• Molecular Weight: 161.15738
• Product Categories: ACETYLGROUP
• Mol File: 1129-36-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyanic acid, 4-acetylphenyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyanic acid, 4-acetylphenyl ester (9CI)(1129-36-8)
• EPA Substance Registry System: Cyanic acid, 4-acetylphenyl ester (9CI)(1129-36-8)

Safety Data

• Hazardous Substances Data: 1129-36-8(Hazardous Substances Data)

Upstream product

• 99-93-4 4-Hydroxyacetophenone 
• 506-77-4 cyanogen chloride 
• 506-68-3 bromocyane 

Downstream Products

• 1091-07-2 N-p-Tolyl-O-<4-acetyl-phenyl>-isoharnstoff 
• 721-94-8 Kohlensaeure-(4-acetyl-phenylester)-imid-(β,β-dimethyl-hydrazid) 
• 5725-04-2 Nβ-<4-Acetyl-phenoxycarbimidoyl>-benzolsulfonsaeure-hydrazid 
• 5725-18-8 Nα-<4-Acetyl-phenoxycarbimidoyl>-benzolsulfonsaeure-hydrazid 
• 5762-71-0 Kohlensaeure-O-<4-acetyl-phenylester>-imid- 
• 3277-43-8 Kohlensaeure-(4-acetyl-phenylester)-imid-cyanamid 
• 3879-50-3 Kohlensaeure-(4-acetyl-phenylester)-imid-(3,4-dichlor-phenyl-cyanamid) 
• 3509-63-5 Semicarbazid-carbimidsaeure-⁽¹⁾-(4-acetyl-phenylester) 
• 3514-98-5 Kohlensaeure-<4-acetyl-phenylester>-imid- 
• 3174-97-8 Iminokohlensaeure-(4-acetyl-phenylester)-hydroxylamid 
• 1132-70-3 Thiocarbamidsaeure-O-<4-acetyl-phenylester> 
• 4612-89-9 2-(4-morpholinyl)-1-cyclohexene-1-carbonitrile 
• 31879-47-7 2-benzoyl-3-oxo-3-phenylpropanenitrile 
• 52805-60-4 C₂₀H₂₃N₃O₃ 

Relevant articles and documents

Improved organocatalytic electrophilic α-cyanation of β-keto amides with 1-cyanato-4-nitrobenzene

By using a readily accessible, new and safe cyano-transfer reagent, 1-cyanato-4-nitrobenzene, the enantioselectivity of the direct electrophilic α-cyanation of 1-indanone-derived β-keto amides was greatly improved as a result of an enhanced double-hydroge

Enantioselective electrophilic cyanation of β-keto amides catalysed by a cinchona organocatalyst

An operationally simple protocol for the enantioselective electrophilic α-cyanation of β-keto amides catalyzed by cinchona-derived catalysts has been demonstrated. The resulting products could be obtained with good to high enantioselectivities (up to 88% ee) and with excellent yields (up to 94%) by employing the mild active 4-acetylphenyl cyanate as the cationic cyano source in the catalytic asymmetric α-cyanation reaction.