50544-72-4

Usage

Uses

Used in Pharmaceutical Drug Development:
7-HYDROXY-2,2,8-TRIMETHYL-2,3-DIHYDRO-4H-CHROMEN-4-ONE is used as a key component in the development of pharmaceutical drugs due to its potential pharmacological and biological activities. Its unique structure allows it to be a promising candidate for the treatment of various medical conditions.
Used in Medicinal and Therapeutic Fields:
In the medicinal and therapeutic fields, 7-HYDROXY-2,2,8-TRIMETHYL-2,3-DIHYDRO-4H-CHROMEN-4-ONE is used for its potential applications in treating various health issues. Its unique structure and properties make it a valuable asset in the development of new therapies and treatments.
Used in the Food Industry:
7-HYDROXY-2,2,8-TRIMETHYL-2,3-DIHYDRO-4H-CHROMEN-4-ONE is used in the food industry as an antioxidant. Its highly oxygenated structure provides it with antioxidant properties, which can help preserve the quality and freshness of food products.
Used in the Cosmetic Industry:
In the cosmetic industry, 7-HYDROXY-2,2,8-TRIMETHYL-2,3-DIHYDRO-4H-CHROMEN-4-ONE is used for its potential beneficial properties. Its unique structure and properties may contribute to the development of cosmetics with enhanced benefits for skin health and appearance.
Further research and studies are needed to explore the full range of applications and potential benefits of 7-HYDROXY-2,2,8-TRIMETHYL-2,3-DIHYDRO-4H-CHROMEN-4-ONE in various industries. Its unique structure and potential pharmacological and biological activities make it a valuable compound for future development and innovation.

InChI:InChI=1/C12H14O3/c1-7-9(13)5-4-8-10(14)6-12(2,3)15-11(7)8/h4-5,13H,6H2,1-3H3

Upstream product

• 541-47-9 3-Methylbutenoic acid 
• 608-25-3 2-methylbenzene-1,3-diol 
• 121485-17-4 1-(2,4-Dihydroxy-3-methyl-phenyl)-3-methyl-but-2-en-1-one 

Downstream Products

• 133035-44-6 N-(2,6-Diethyl-phenyl)-2-(2,2,8-trimethyl-4-oxo-chroman-7-yloxy)-acetamide 
• 133035-43-5 N-(2-Ethyl-6-methyl-phenyl)-2-(2,2,8-trimethyl-4-oxo-chroman-7-yloxy)-acetamide 
• 133035-39-9 N-Phenyl-2-(2,2,8-trimethyl-4-oxo-chroman-7-yloxy)-acetamide 
• 133035-42-4 N-(2-Chloro-phenyl)-2-(2,2,8-trimethyl-4-oxo-chroman-7-yloxy)-acetamide 
• 121485-25-4 7-Cyclohexyloxy-2,2,8-trimethyl-chroman-4-one 
• 121485-28-7 7-(4-Chloro-benzyloxy)-2,2,8-trimethyl-chroman-4-one 
• 121485-27-6 7-(2-Chloro-benzyloxy)-2,2,8-trimethyl-chroman-4-one 
• 131859-54-6 7-(4-Bromo-benzyloxy)-2,2,8-trimethyl-2H-chromene 
• 133035-98-0 N-Phenyl-2-(2,2,8-trimethyl-2H-chromen-7-yloxy)-acetamide 
• 131859-40-0 7-(4-Bromo-benzyloxy)-2,2,8-trimethyl-chroman-4-ol 
• 131859-56-8 2,2,8-Trimethyl-7-(4-nitro-benzyloxy)-2H-chromene 
• 133036-00-7 N-p-Tolyl-2-(2,2,8-trimethyl-2H-chromen-7-yloxy)-acetamide 
• 133035-99-1 N-o-Tolyl-2-(2,2,8-trimethyl-2H-chromen-7-yloxy)-acetamide 
• 133036-01-8 N-(2-Chloro-phenyl)-2-(2,2,8-trimethyl-2H-chromen-7-yloxy)-acetamide 

Relevant academic research and scientific papers

SYNTHESIS OF ANALOGUES OF NATURAL PRECOCENES CONTAINING A 8-METHYL SUBSTITUENT

The synthesis of benzopyran compounds (VIIIa-q), analogues of precocene I (I) substituted on C-8 in the aromatic ring with a methyl group, is described.

Pyranochromone derivatives and therapeutic composition comprising same for treatment of allergic diseases

Novel pyranochromone derivatives having the general formula: STR1 wherein R1 represents hydrogen atom, an alkali metal or an alkyl group containing 1-4 carbon atoms; R2, R3 and R4 represent hydrogen atom or an alkyl group containing 1-4 carbon atoms respectively, provided that both R3 and R4 are not hydrogen atom at the same time; R5 and R6 represent an alkyl group containing 1-4 carbon atoms respectively; and R7 represents hydrogen atom, hydroxyl group, an alkyl group containing 1-4 carbon atoms or an alkoxyl group containing 1-4 carbon atoms. The novel medicaments comprising predominantly the above derivative are effective for the treatment of allergic diseases.