32268-30-7

Basic information

• Product Name: Benzaldehyde, 2,4-dihydroxy-3-(3-methyl-2-butenyl)-
• CAS NO: 32268-30-7
• Molecular Formula: C12H14O3
• Molecular Weight: 206.241
• Mol File: 32268-30-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2,4-dihydroxy-3-(3-methyl-2-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2,4-dihydroxy-3-(3-methyl-2-butenyl)-(32268-30-7)
• EPA Substance Registry System: Benzaldehyde, 2,4-dihydroxy-3-(3-methyl-2-butenyl)-(32268-30-7)

Safety Data

• Hazardous Substances Data: 32268-30-7(Hazardous Substances Data)

Upstream product

• 115-18-4 2-methyl-3-buten-2-ol 
• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 163041-67-6 2-hydroxy-3-(3-methylbut-2-en-1-yl)-4-[(tetrahydro-2H-pyran-2-yl)oxy]benzaldehyde 
• 870-63-3 prenyl bromide 

Downstream Products

• 263902-83-6 3-benzoyl-8,8-dimethyl-8H-pyrano[2,3-f]chromen-2-one 
• 310403-17-9 8,8-dimethyl-3-(4-nitro-benzoyl)-8H-pyrano[2,3-f]chromen-2-one 
• 144506-14-9 Licochalcone C 
• 163041-69-8 2-methoxy-3-(3-methylbut-2-en-1-yl)-4-[(tetrahydro-2H-pyran-2-yl)oxy]benzaldehyde 
• 163041-67-6 2-hydroxy-3-(3-methylbut-2-en-1-yl)-4-[(tetrahydro-2H-pyran-2-yl)oxy]benzaldehyde 
• 144506-14-9 licochalcone 
• 523-59-1 seseline 
• 54287-99-9 5-hydroxy-2,2-dimethyl-2H-chromene-6-carbaldehyde 

Relevant articles and documents

Synthetic methods for Gramniphenols F and G, Cicerfuran, Morunigrol C and its Derivative

The present invention relates to a method for preparing natural benzofurans including gramniphenol F, gramniphenol G, morunigrol C and 3andprime;,5andprime;-di-O-methyl analogues thereof and cicerfuran by using 2,4-dihydroxybenzaldehyde, 5-bromoresorcinol and sesamol. In the method according to the present invention, region-selective prenylation, Ramirez gem-dibromo olefination, Miyaura borylation and Suzuki coupling are used. In addition, the compounds were determined for anti-inflammatory effects through a test for production of nitrogen oxide in liposaccharide-induced RAW-264.7 macrophages. All of the compounds show weak to medium (16-42%) inhibitory activities, are not toxic and have an IC_50 value of 9.1 to 25.2 andmu;M.COPYRIGHT KIPO 2017

Facile synthesis of licochalcone C

Licochalcone C was synthesized from commercially available 2,4-dihydroxybenzaldehde by using regioselective Al2O 3-mediated C-prenylation followed by conventional Claisen-Schmidt condensation in basic condition.

THERAPEUTIC AGENT

A therapeutic agent and prophylactic agent for a disease accompanying an abnormality in an amount of insulin or insulin response, an agent for an insulin-mimetic action, a food, beverage and feed, an agent for enhancing glucose uptake into a cell, and an agent for inducing differentiation into an adipocyte, characterized in that each comprises as an effective ingredient at least one compound selected from the group consisting of a chalcone compound, an acetophenone compound, a coumarin compound, a phthalide compound, derivatives thereof, and pharmacologically acceptable salts thereof.