66016-88-4

Basic information

• Product Name: Dimethyl-3-chloro-2-pentenedioate
• Synonyms: Dimethyl-3-chloro-2-pentenedioate
• CAS NO: 66016-88-4
• Molecular Formula: C₇H₉ClO₄
• Molecular Weight: 192.59696
• Mol File: 66016-88-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 239.1±30.0 °C(Predicted)
• Appearance: /
• Density: 1.235±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Dimethyl-3-chloro-2-pentenedioate(CAS DataBase Reference)
• NIST Chemistry Reference: Dimethyl-3-chloro-2-pentenedioate(66016-88-4)
• EPA Substance Registry System: Dimethyl-3-chloro-2-pentenedioate(66016-88-4)

Safety Data

• Hazardous Substances Data: 66016-88-4(Hazardous Substances Data)

Upstream product

• 1830-54-2 3-oxopentanedioic acid dimethyl ester 

Downstream Products

• 125981-69-3 methyl (6-p-bromophenyl-3-methoxycarbonyl-5-phenyl-2H-thiopyran-2-ylidene)acetate 
• 131124-15-7 2-[1-Methoxycarbonyl-meth-(Z)-ylidene]-5-phenyl-6-trifluoromethyl-2H-thiopyran-3-carboxylic acid methyl ester 
• 125981-66-0 methyl (6-p-bromophenyl-3-methoxycarbonyl-2H-thiopyran-2-ylidene)acetate 
• 125981-67-1 methyl (3-methoxycarbonyl-6-p-methoxyphenyl-2H-thiopyran-2-ylidene)acetate 
• 125981-68-2 methyl 2-methoxycarbonylmethylen-5,6-diphenyl-2H-thiopyran-3-carboxylate 
• 125981-65-9 methyl (6-p-chlorophenyl-3-methoxycarbonyl-2H-thiopyran-2-ylidene)acetate 
• 125981-60-4 methyl (3-methoxycarbonyl-6-phenyl-2H-thiopyran-2-ylidene)acetate 

Relevant articles and documents

A practical improvement of crystallization-induced asymmetric transformation of allene-1,3-dicarboxylates

Enantiomerically pure allene-1,3-dicarboxylates were easily synthesized by using epimerization-crystallization of dissymmetric allene compounds, which were prepared from acetone-1,3-dicarboxylates and naturally abundant chiral alcohols, that is, (-)- and

THE CHEMISTRY OF STABILIZED 2H-THIOPYRANES

2H-Thiopyranes with a side chain in position 2 of the ring and a terminal formyl group are resonance stabilized compounds.They represent solid, coloured substances, both thermal stable and also reactive, especially against several nucleophilic reagents.Th