1262033-05-5

Basic information

• Product Name: C₁₆H₂₀Cl₂O₄
• Synonyms: C₁₆H₂₀Cl₂O₄
• CAS NO: 1262033-05-5
• Molecular Weight: 347.238
• Mol File: 1262033-05-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₆H₂₀Cl₂O₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₆H₂₀Cl₂O₄(1262033-05-5)
• EPA Substance Registry System: C₁₆H₂₀Cl₂O₄(1262033-05-5)

Safety Data

• Hazardous Substances Data: 1262033-05-5(Hazardous Substances Data)

Upstream product

• 51335-75-2 2,2-Dimethyl-1,3-dioxacyclohexane-5,5-dicarboxylic acid,diethyl ester 
• 82962-54-7 2,2-dimethyl-5-ethoxycarbonyl-1,3-dioxane 
• 4728-12-5 2,2-dimethyl-5-hydroxymethyl-1,3-dioxane 

Downstream Products

• 1262033-17-9 C₁₂H₁₂Cl₂O₃ 
• 1262033-23-7 C₁₂H₁₀Cl₂O₃ 
• 1262032-89-2 5-acetyloxymethyl-3-(3,4-dichlorophenyl)-5,6-dihydro-2H-pyran-2-one 
• 1262032-91-6 C₁₇H₁₈Cl₂O₄ 
• 1262032-92-7 C₁₉H₁₄Cl₂O₄ 
• 1262033-11-3 C₁₃H₁₆Cl₂O₄ 

Relevant articles and documents

3,5-Disubstituted pyranone analogues of highly antifungally active furanones: Conversion of biological effect from antifungal to cytostatic

A series of 3-aryl-5-acyloxymethyl-5,6-dihydro-2H-pyran-2-ones, related to highly antifungally active butenolides, was synthesized via cyclization of substituted δ-hydroxy acids as the key step, and evaluated for their in vitro antifungal activity and cytostatic activity. While the extension of the furanone ring to pyranone led to a complete loss of the antifungal effect, some of the compounds displayed promising effect against several cell lines, including the resistant colorectal carcinoma cells.