2999-37-3

Basic information

• Product Name: 1-Butanone, 1-(2-hydroxy-4,6-dimethoxyphenyl)-
• CAS NO: 2999-37-3
• Molecular Formula: C12H16O4
• Molecular Weight: 224.257
• Mol File: 2999-37-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Butanone, 1-(2-hydroxy-4,6-dimethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanone, 1-(2-hydroxy-4,6-dimethoxyphenyl)-(2999-37-3)
• EPA Substance Registry System: 1-Butanone, 1-(2-hydroxy-4,6-dimethoxyphenyl)-(2999-37-3)

Safety Data

• Hazardous Substances Data: 2999-37-3(Hazardous Substances Data)

Usage

Derivation

Derived from the guaiacol molecule

Usage

Commonly used as a flavoring agent in food and beverages due to its sweet, vanilla-like aroma

Production

Utilized in the production of vanilla extracts and synthetic vanilla flavorings

Applications

Has applications in the fragrance industry, as well as in the synthesis of pharmaceuticals and other organic compounds

Importance

Unique properties and versatile uses make it an important chemical in various industries.

Upstream product

• 500-99-2 3,5-dimethoxyphenol 
• 109-74-0 propyl cyanide 
• 2437-62-9 1-(2,4,6-trihydroxyphenyl)butan-1-one 
• 80-48-8 methyl p-toluene sulfonate 
• 1203549-54-5 3,5-dimethoxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 107-92-6 butyric acid 
• 621-23-8 1,2,3-trimethoxybenzene 
• 108-73-6 3,5-dihydroxyphenol 
• 77-78-1 dimethyl sulfate 
• 76569-40-9 1-(2,4,6-trimethoxyphenyl)-1-butanone 
• 326854-40-4 1-(2,4-dimethoxy-6-triisopropylsilanyloxy-phenyl)-butan-1-one 
• 62995-12-4 1-(2-hydroxy-4,6-dimethoxyphenyl)but-2-en-1-one 

Downstream Products

• 326854-41-5 1-(2-hydroxy-4-methoxy-6-triisopropylsilanyloxy-phenyl)-butan-1-one 
• 531502-71-3 8-butyl-5,7-dimethoxy-2-(3',4',5'-trimethoxyphenyl)-4H-chromen-4-one 
• 531502-62-2 1-(3-butyl-2-hydroxy-4,6-dimethoxy-phenyl)-ethanone 
• 326854-40-4 1-(2,4-dimethoxy-6-triisopropylsilanyloxy-phenyl)-butan-1-one 
• 66346-55-2 5,7-dimethoxy-4-propyl-2H-1-benzopyran-2-one 

Relevant articles and documents

Solvent effects on stereoselectivity in 2,3-dimethyl-4-chromanone cyclization by quinine-catalyzed asymmetric intramolecular oxo-Michael addition

Examination of the quinine-catalyzed asymmetric intramolecular oxo-Michael addition of o-tigloylphenol in various solvents led to high stereoselectivity in chromanone cyclization when chlorobenzene was used as a solvent, giving cis-2,3-dimethyl-4-chromano

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

Enantioselective total synthesis of anti HIV-1 active (+)-calanolide A through a quinine-catalyzed asymmetric intramolecular oxo-Michael addition

Enantioselective total synthesis of anti HIV-1 active (+)-calanolide A was achieved by a quinine-catalyzed asymmetric intramolecular oxo-Michael addition as a key step. (C) 2000 Elsevier Science Ltd.