65383-61-1

Basic information

• Product Name: 6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE
• Synonyms: 2,3-dihydro-6,7-dimethoxy-2,2-dimethyl-4h-1-benzopyran-4-on;6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE;6,7-dimethoxy-2,2-dimethyl-4-chromanone;2,3-dihydro-6,7-dimethoxy-2,2-dimethyl-4H-1-benzopyran-4-one;6,7-dimethoxy-2,2-dimethylchroman-4-one;6,7-dimethoxy-2,2-dimethyl-3H-chromen-4-one
• CAS NO: 65383-61-1
• Molecular Formula: C₁₃H₁₆O₄
• Molecular Weight: 236.26
• EINECS: 265-726-4
• Product Categories: Heterocyclic Compounds;Benzopyrans;Building Blocks;Heterocyclic Building Blocks
• Mol File: 65383-61-1.mol
• Article Data: 13

Chemical Properties

• Melting Point: 105-107 °C(lit.)
• Boiling Point: 357.6°C at 760 mmHg
• Flash Point: 158°C
• Appearance: /
• Density: 1.123g/cm³
• Vapor Pressure: 2.69E-05mmHg at 25°C
• Refractive Index: 1.509
• CAS DataBase Reference: 6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE(65383-61-1)
• EPA Substance Registry System: 6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE(65383-61-1)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 65383-61-1(Hazardous Substances Data)

Usage

Uses

6,7-Dimethoxy-2,2-dimethyl-4-chromanone was used to examine the response of P. sojae zoospores to a wide range of compounds having some structural similarity to genistein and daidzein.

InChI:InChI=1/C13H16O4/c1-13(2)7-9(14)8-5-11(15-3)12(16-4)6-10(8)17-13/h5-6H,7H2,1-4H3

Upstream product

• 20628-06-2 2-hydroxy-4,5-dimethoxyacetophenone 
• 67-64-1 acetone 
• 541-47-9 3-Methylbutenoic acid 
• 866252-52-0 4,5-dimethoxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 1818-28-6 2',4',5'-trimethoxyacetophenone 
• 112979-30-3 3,4-dioxymethylene phenyl 3-methyl-2-butenoate 
• 112979-31-4 1-(2-hydroxy-4,5-methylenedioxyphenyl)-3-methyl-2-buten-1-one 
• 73673-87-7 2,2-dimethyl-6,7-methylenedioxy-4-chromanone 
• 74094-44-3 2,2-Dimethyl-6-hydroxy-7-methoxy-4-chromanone 
• 74-88-4 methyl iodide 
• 76348-95-3 2,2-Dimethyl-6,7-dihydroxy-4-chromanone 
• 77607-80-8 1-(2'-hydroxy-4',5'-dimethoxyphenyl)-3-hydroxy-3-methyl-butan-1-one 
• 97024-81-2 1-(2-hydroxy-4,5-dimethoxyphenyl)-3-methyl-2-buten-1-one 

Downstream Products

• 76348-95-3 2,2-Dimethyl-6,7-dihydroxy-4-chromanone 
• 131859-58-0 2,2-dimethyl-6,7-bis((4-nitrobenzyl)oxy)-2H-chromene 
• 131859-43-3 2,2-dimethyl-6,7-bis((4-nitrobenzyl)oxy)chroman-4-ol 
• 94245-01-9 6,7-dibenzyloxy-2,2-dimethyl-4-chromanone 

Relevant articles and documents

β,β-DIMETHYLACRYLOPHENONES AND A CHROMANONE FROM NAMA HISPIDUM AND J. JOHNSTONII

A β,β-dimethacrylophenone and the corresponding chromanone were isolated from the leaf resin of Nama hispidum.The leaf exudate of N. johnstonii contains another β,β-dimethacrylophenone as colouring matter.Key Word Index - Nama hispidum; N. johnstonii; Hydrophyllaceae; leaf resin; dimethacrylophenones; chromanone.

Intermolecular C-O addition of carboxylic acids to arynes: Synthesis of o-hydroxyaryl ketones, xanthones, 4-chromanones, and flavones

An efficient and simple route to biologically and pharmaceutically important o-hydroxyaryl ketones, xanthones, 4-chromanones, and flavones has been developed utilizing readily available carboxylic acids and commercially available o-(trimethylsilyl)aryl tr

Intermolecular C-O addition of carboxylic acids to arynes

(Figure Presented) A novel, efficient, and expedient route to biologically and pharmaceutically important o-hydroxyaryl ketones, xanthones, 4-chromanones, and flavones has been developed starting from readily available carboxylic acids and commercially available o-(trimethylsilyl)aryl triflates.