55198-61-3

Basic information

• Product Name: N-(3,5-dichlorophenyl)maleamic acid
• Synonyms: N-(3,5-dichlorophenyl)maleamic acid;(Z)-4-((3,5-dichlorophenyl)amino)-4-oxobut-2-enoic acid;(2Z)-4-((3,5-dichlorophenyl)amino)-4-oxobut-2-enoic acid
• CAS NO: 55198-61-3
• Molecular Formula: C₁₀H₇Cl₂NO₃
• Molecular Weight: 260.07
• Mol File: 55198-61-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 483°C at 760 mmHg
• Flash Point: 245.9°C
• Appearance: /
• Density: 1.551g/cm³
• Vapor Pressure: 3.84E-10mmHg at 25°C
• Refractive Index: 1.65
• CAS DataBase Reference: N-(3,5-dichlorophenyl)maleamic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,5-dichlorophenyl)maleamic acid(55198-61-3)
• EPA Substance Registry System: N-(3,5-dichlorophenyl)maleamic acid(55198-61-3)

Safety Data

• Hazardous Substances Data: 55198-61-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H7Cl2NO3/c11-6-3-7(12)5-8(4-6)13-9(14)1-2-10(15)16/h1-5H,(H,13,14)(H,15,16)/b2-1-

Upstream product

• 108-31-6 maleic anhydride 
• 626-43-7 3,5-Dichloroaniline 

Downstream Products

• 1313395-77-5 N⁽¹⁾-(3,5-dichlorophenyl)-N⁽⁴⁾-(2-methoxyphenyl)fumaramide 
• 1313395-66-2 N⁽¹⁾-(3,5-dichlorophenyl)-N⁽⁴⁾-(2-methoxyphenyl)maleamide 
• 24096-52-4 1-(3,5-dichlorophenyl)-2,5-dihydro-1H-pyrrole-2,5-dione 

Relevant articles and documents

DABCO-catalyzed [3+2] cycloaddition reactions of azomethine imines with N-aryl maleimides: Facile access to dinitrogen-fused heterocycles

DABCO-catalyzed [3+2] cycloaddition of azomethine imines with maleimides has been developed. This method could efficiently furnish dinitrogen-fused tetracyclic heterocycles in high levels of regioselectivity and with good yields.

Antimicrobial composition and method containing N-(3,5-dihalophenyl)-imide compounds

Novel N-(3,5-dihalophenyl)imide compounds, which exhibit a strong antimicrobial activity against microorganisms including phytopathogenic fungi, parasites of industrial products and pathogenic microorganisms, represented by the formula, STR1 wherein X and X' each represent halogens and A represents a substituted ethylene such as chloroethylene, C1 - C4 alkylthioethylene, C1 - C2 alkyl-ethylene or 1,2-di-C1 - C2 -alkyl-ethylene, a cyclopropylene such as 1,3-dimethylcyclopropylene, trimethylene, a cyclohexylene-1,2-, cyclohexenylene-1,2-, cyclohexadienylene-1,2- or o-phenylene. The N-(3,5-dihalophenyl)imide compounds can be obtained by any of methods which produce imide compounds or reaction of an N-(3,5-dihalophenyl)maleimide compound with a mercaptan, a hydrogen halide, phosphorus chloride or thionylchloride.