20921-01-1

Basic information

• Product Name: 7-methylchroman-2-one
• Synonyms: 7-methylchroman-2-one
• CAS NO: 20921-01-1
• Molecular Formula: C₁₀H₁₀O₂
• Molecular Weight: 162.1852
• Mol File: 20921-01-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 291.1°Cat760mmHg
• Flash Point: 117.8°C
• Appearance: /
• Density: 1.157g/cm³
• Vapor Pressure: 0.00199mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: 7-methylchroman-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-methylchroman-2-one(20921-01-1)
• EPA Substance Registry System: 7-methylchroman-2-one(20921-01-1)

Safety Data

• Hazardous Substances Data: 20921-01-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H10O2/c1-7-2-3-8-4-5-10(11)12-9(8)6-7/h2-3,6H,4-5H2,1H3

Upstream product

• 288310-94-1 1,1,1-trifluoro-4-(4-methylphenyl)butan-2-one 

Downstream Products

• 1424179-23-6 C₁₄H₂₀O₂ 
• 1392825-08-9 10-hydroxy-2-methyl-11-oxo-11H-benzo[b]fluorene-4,9-diyl dibenzenesulfonate 
• 1392825-15-8 C₃₂H₂₇NO₁₁S₂ 
• 1392825-07-8 C₁₆H₁₂O₄S 
• 1392825-14-7 C₁₆H₁₄O₄S 
• 117008-05-6 (E)-5-(1-Acetoxy-4-methyl-6-oxo-cyclohexa-2,4-dienyl)-pent-2-enoic acid ethyl ester 
• 85960-58-3 ethyl 5-(2-hydroxy-4-methylphenyl)-2-pentenoate 
• 20921-13-5 ethyl 3-(2-hydroxy-4-methylphenyl)propanoate 

Relevant articles and documents

Regioselective intramolecular oxidation of phenols and anisoles by dioxiranes generated in situ

A novel method for regioselective oxidation of phenols and anisoles has been developed in which dioxiranes, generated in situ from ketones and Ozone, oxidize phenol derivatives in an intramolecular fashion. A series of ketones with electron-withdrawing groups, such as CF3, COOMe, and CH2Cl, were attached to phenols, anisoles, or aryl rings via a C2 or C3 methylene linker. In a homogeneous solvent system of CH3CN and H2O, oxidation of phenol derivatives 1-10 afforded spiro 2-hydroxydienones in 24-55% yields regardless of the presence of other substituents (ortho Me, meta Me or Br) on the aryl ring and the length of the linker. Experimental evidences were provided to support the mechanism that involves a regioselective π bond epoxidation of aryl rings followed by epoxide rearrangement and hemiketal formation.