24962-85-4

Basic information

• Product Name: 2(3H)-Furanone, dihydro-5-(4-methoxybenzoyl)-
• CAS NO: 24962-85-4
• Molecular Formula: C12H12O4
• Molecular Weight: 220.225
• Mol File: 24962-85-4.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2(3H)-Furanone, dihydro-5-(4-methoxybenzoyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Furanone, dihydro-5-(4-methoxybenzoyl)-(24962-85-4)
• EPA Substance Registry System: 2(3H)-Furanone, dihydro-5-(4-methoxybenzoyl)-(24962-85-4)

Safety Data

• Hazardous Substances Data: 24962-85-4(Hazardous Substances Data)

Upstream product

• 696-62-8 para-iodoanisole 
• 146744-35-6 (1S,2R)-trans-2-(4-methoxyphenyl)cyclohexanol 
• 591-80-0 pent-4-enoic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 5724-06-1 (4E)-5-(4-methoxyphenyl)pent-4-enoic acid 
• 100-66-3 methoxybenzene 
• 108-55-4 glutaric anhydride, 
• 729580-61-4 ethyl 5-(4-methoxylphenyl)-4-pentynoate 
• 63093-41-4 ethyl 4-pentynoate 
• 6089-09-4 4-pentynoic acid 
• 137742-44-0 5-<4-methoxyphenyl>-4-pentynoic acid 
• 4609-10-3 5-(4-methoxyphenyl)-5-oxopentanoic acid 

Relevant articles and documents

Phenyliodine(III) triflate mediated synthesis of 5-benzoyldihydro-2(3H)- furanones

A direct and efficient method for the preparation of 5-benzoyldihydro-2(3H) -furanones was realized by cyclization of 4-benzoylbutyric acids in the presence of phenyliodine(III) triflate.

Visible-Light-Promoted Metal-Free Aerobic Oxidation of Primary Amines to Acids and Lactones

A unique metal-free aerobic oxidation of primary amines via visible light photocatalytic double carbon–carbon bonds cleavage and multi carbon–hydrogen bonds oxidation was observed. Aerobic oxidation of primary amines could be controlled to afford acids by using dioxane with 18 W CFL, and lactones by using DMF with 8 W green LEDs, respectively. A plausible mechanism was proposed based on control experiments. This observation showed direct evidences for the fragmentation in the aerobic oxidation of aliphatic primary amines.

Calcium iodide catalyzed photooxidative oxylactonization of oxocarboxylic acids using molecular oxygen as terminal oxidant

We developed aerobic photooxidative oxylactonization of oxocarboxylic acids catalyzed by calcium iodide using molecular oxygen as the terminal oxidant under photo irradiation.