1124-59-0

Basic information

• Product Name: Cyanic acid, 4-chlorophenyl ester
• CAS NO: 1124-59-0
• Molecular Formula: C7H4ClNO
• Molecular Weight: 153.568
• Mol File: 1124-59-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Cyanic acid, 4-chlorophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Cyanic acid, 4-chlorophenyl ester(1124-59-0)
• EPA Substance Registry System: Cyanic acid, 4-chlorophenyl ester(1124-59-0)

Safety Data

• Hazardous Substances Data: 1124-59-0(Hazardous Substances Data)

Upstream product

• 93049-43-5 5-(4-chlorophenyloxy)-1,2,3,4-thiatriazole 
• 506-68-3 bromocyane 
• 106-48-9 4-chloro-phenol 
• 937-64-4 4-chlorophenyl chlorothionoformate 
• 506-77-4 cyanogen chloride 

Downstream Products

• 61854-09-9 p-Chlorphenyl-N-(isocyanatocarbonyl)-chlorcarbonimidat 
• 7121-20-2 4-Methoxy-O-<4-chlor-phenoxycarbimidoyl>-benzaldoxim 
• 40588-10-1 Kohlensaeure-methylester-(p-chlorphenyl)esterimid 
• 7026-24-6 O-<4-Chlor-phenoxy-carbimidoyl>-acetophenonoxim 
• 7026-19-9 O-<4-Chlor-phenoxy-carbimidoyl>-cyclohexanonoxim 
• 16936-56-4 4-chlorophenyl trichloromethyl ether 
• 7026-20-2 O-(4-Chlor-phenoxy-carbimidoyl)-benzophenonoxim 
• 7200-67-1 2-Methyl-O-(4-chlor-phenoxycarbamidoyl)-benzochinon-1-monoxim 
• 7050-81-9 4-Chlor-O-<4-chlor-phenoxycarbimidoyl>-benzaldoxim 
• 4611-43-2 5-(4-chlorophenoxy)tetrazole 
• 24641-61-0 O-(4-chlorophenyl) thiocarbamate 
• 1352031-55-0 5-(4-chlorophenoxy)-1,2,4-dithiazole-3-one 
• 22071-63-2 N.N'-Ethyliden-bis- 
• 22100-93-2 N.N'-Methylen-bis- 

Relevant articles and documents

Oxidative rearrangement strategy for synthesis of 2,4,5-trisubstituted oxazoles utilizing hypervalent iodine reagent

Hypervalent iodine (III)-intermediated direct oxidative rearrangement of 3-hydroxybut-2-enimidates affording oxazoles under mild conditions has been developed. This protocol provides a new methodology to the synthesis of compounds containing oxazole structure.

Synthesis and structure of substituted 5-phenoxy-1,2,4-dithiazole-3-ones

Seven new substituted 5-phenoxy-1,2,4-dithiazole-3-ones were prepared in modest yield (53-76%) from corresponding O-phenyl thiocarbamates and chlorocarbonylsulfenyl chloride in dry ether at-10 °C. All of the compounds were characterized by NMR and elemental analysis and some of them by X-ray diffraction. Preliminary kinetic measurements showed that the parent 5-phenoxy-1,2,4-dithiazole-3-one is a very efficient sulfurizing agent toward triphenyl phosphite. Copyright

Interaction of aryloxychlorocarbenes with acetylenedicarboxylate: Novel formation of polyfunctional butadienes and 8-oxatricyclo[3.2.1.0 2.4]oct-6-enes

The interaction of aryloxychlorocarbenes with dialkyl acetylenedicarboxylates has been examined. Thermolyses of 3-aryloxy-3- chlorodiazirines in the presence of acetylenedicarboxylate resulted in the formation of unexpected polyfunctional 1,3-butadienes and 8-oxatricyclo[3.2.1. 02.4]oct-6-enes or of 2-aryoxycarbonylmaleates dependent upon reaction conditions. This work confirmed the nucleophilicity of aryloxychlorocarbenes and underlined their synthetic potential.