617-42-5

Basic information

• Product Name: 2-chloromaleic acid
• Synonyms: 2-chloromaleic acid;(Z)-2-Chloro-2-butenedioic acid;2-Butenedioic acid, 2-chloro-, (Z)-;Fumaric acid, chloro-;Nsc42913;Wln: qvygu1vq -t
• CAS NO: 617-42-5
• Molecular Formula: C₄H₃ClO₄
• Molecular Weight: 150.52
• Mol File: 617-42-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 326°C at 760 mmHg
• Flash Point: 151°C
• Appearance: /
• Density: 1.698g/cm³
• Vapor Pressure: 4.45E-05mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: 2-chloromaleic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloromaleic acid(617-42-5)
• EPA Substance Registry System: 2-chloromaleic acid(617-42-5)

Safety Data

• Hazardous Substances Data: 617-42-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C4H3ClO4/c5-2(4(8)9)1-3(6)7/h1H,(H,6,7)(H,8,9)/b2-1+

Upstream product

• 6677-58-3 β-Chlor-β-carboxy-acrylsaeureamid 
• 88-06-2 2,4,6-Trichlorophenol 
• 3856-37-9 (2R,3S)-2,3-Dichloro-succinic acid 
• 7664-93-9 sulfuric acid 
• 7647-01-0 hydrogenchloride 
• 6910-76-5 monochloromaleonitrile 
• 1114-09-6 d,l-dichlorosuccinic acid 
• 7732-18-5 water 
• 71200-79-8 chlorofumarodinitrile 
• 1114-09-6 d-dichlorosuccinic acid 
• 89180-55-2 2,3,4,4,4-pentachloro-butyric acid 
• 88497-26-1 2-bromo-3-chloro-succinic acid 
• 2257-39-8 3,4,4-trichloro-2-hydroxy-but-3-enoic acid 
• 617-43-6 2-chloromaleic acid 

Downstream Products

• 10302-94-0 (Z)-2-chloro-2-butenedioic acid, diethyl ester 
• 96-02-6 2-chloromaleic anhydride 
• 617-43-6 2-chloromaleic acid 
• 73257-73-5 3,3,3-trichloro-2,2-dihydroxy-propionic acid 
• 13797-26-7 3-anilino-1-phenyl-pyrrole-2,5-dione 
• 110-15-6 succinic acid 
• 7732-18-5 water 
• 4198-33-8 (2S)-chlorobutanedioic acid 
• 22801-48-5 n-Butyl-chlorfumarat 
• 22801-46-3 n-Propyl-chlorfumarat 

Relevant articles and documents

Metallophthalocyanines linked to organic copolymers as efficient oxidative supported catalysts

The covalent anchoring of metallo(chlorosulfonyl)phthalocyanines 1 onto the acrylic copolymers 2 and 3 has been achieved. When using H2O2 or KHSO5 as oxidant, these supported catalysts are able to oxidize a poorly biodegradable molecule such as 2,4,6-trichlorophenol or a tannin model such as 3,5-di-tert-butylcatechol. The influence of the spacer and the nature of the reaction medium on the catalytic activities have been studied, as well as the recycling of these supported metallophthalocyanine catalysts.

Purification and properties of crystalline 3-methylaspartase from two facultative anaerobes, Citrobacter sp. strain YG-0504 and Morganella morganii strain YG-0601

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Enantiospecific synthesis of 3-substituted aspartic acids via enzymic amination of substituted fumaric acids

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