1026692-54-5

Basic information

• Product Name: 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one
• Synonyms: 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one
• CAS NO: 1026692-54-5
• Molecular Formula: C₁₂H₁₄O₃
• Molecular Weight: 206.23776
• Mol File: 1026692-54-5.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one(1026692-54-5)
• EPA Substance Registry System: 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one(1026692-54-5)

Safety Data

• Hazardous Substances Data: 1026692-54-5(Hazardous Substances Data)

Usage

Uses

Due to the lack of specific information regarding the properties, uses, and safety of 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one in the provided materials, it is recommended to refer to specialized chemical databases or consult product manufacturers for detailed applications. However, based on its chemical structure and classification, it can be inferred that 2-(4-Methoxyphenyl)dihydro-2H-pyran-4(3H)-one may have potential uses in various industries such as pharmaceuticals, materials science, or chemical research. Further research and testing are necessary to fully understand its characteristics, potential benefits, and risks before it can be applied in specific applications.

Upstream product

• 1206519-72-3 C₁₄H₁₇⁽²⁾HO₄ 
• 1206519-71-2 4-(4-methoxybenzyloxy)but-1-en-2-yl acetate 
• 1206519-73-4 C₁₄H₁₆⁽²⁾H₂O₄ 
• 123-11-5 4-methoxy-benzaldehyde 
• 109553-20-0 3-(phenylthio)but-3-en-1-ol 

Downstream Products

• 1026692-65-8 (2S,4S)-2-(4-methoxyphenyl)-tetrahydro-2H-4-pyranol 

Relevant articles and documents

A novel self-terminated Prins strategy for the synthesis of tetrahydropyran-4-one derivatives and their behaviour in Fisher indole synthesis

A novel self-terminated Prins strategy has been developed for the synthesis of 2-substituted tetrahydropyran-4-one derivatives through a condensation of 3-(phenylthio)but-3-en-1-ol with carbonyl compounds in the presence of 5 mol% of Sc(OTf)3 u

2,3-dichloro-5,6-dicyano-1,4-benzoquinone-catalyzed teactions employing MnO2 as a stoichiometric oxidant

Several oxidative reactions can be effected with MnO2 in the presence of substoichiometric quantities of DDQ. These transformations include oxidative cyclization, deprotection, and dehydrogenation reactions. The use of MnO2 as a terminal oxidant for DDQ-mediated reactions is attractive based on economical and environmental factors.

Mechanistic analysis of oxidative C-H cleavages using inter- and intramolecular kinetic isotope effects

A series of monodeuterated benzylic and allylic ethers were subjected to oxidative carbon-hydrogen bond cleavage to determine the impact of structural variation on intramolecular kinetic isotope effects in DDQ-mediated cyclization reactions. These values