1666-03-1

Basic information

• Product Name: 2-HYDROXY-4,5-DIMETHYL-BENZALDEHYDE
• Synonyms: Salicylaldehyde,4,5-dimethyl- (7CI,8CI); 2-Hydroxy-4,5-dimethylbenzaldehyde;4,5-Dimethylsalicylaldehyde
• CAS NO: 1666-03-1
• Molecular Formula: C₉H₁₀O₂
• Molecular Weight: 150.18
• Mol File: 1666-03-1.mol
• Article Data: 7

Chemical Properties

• Melting Point: 69 °C
• Boiling Point: 243.5°C at 760 mmHg
• Flash Point: 99.8°C
• Appearance: /
• Density: 1.136g/cm³
• Vapor Pressure: 0.0205mmHg at 25°C
• Refractive Index: 1.589
• PKA: 8.60±0.23(Predicted)
• CAS DataBase Reference: 2-HYDROXY-4,5-DIMETHYL-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-HYDROXY-4,5-DIMETHYL-BENZALDEHYDE(1666-03-1)
• EPA Substance Registry System: 2-HYDROXY-4,5-DIMETHYL-BENZALDEHYDE(1666-03-1)

Safety Data

• Hazardous Substances Data: 1666-03-1(Hazardous Substances Data)

Usage

General Description

2-HYDROXY-4,5-DIMETHYL-BENZALDEHYDE is a chemical compound with the molecular formula C9H10O2. It is a derivative of benzaldehyde, containing both hydroxyl and dimethyl substituents. 2-HYDROXY-4,5-DIMETHYL-BENZALDEHYDE is used in the fragrance industry for its sweet, floral, and almond-like aroma. It is also utilized in the production of various pharmaceuticals and as a flavoring agent in food products. Additionally, 2-HYDROXY-4,5-DIMETHYL-BENZALDEHYDE has shown potential antibacterial and antifungal properties, making it of interest for further research in the fields of medicine and microbiology.

InChI:InChI=1/C9H10O2/c1-6-3-8(5-10)9(11)4-7(6)2/h3-5,11H,1-2H3

Upstream product

• 10496-92-1 4,5-dimethyl-2-hydroxybenzyl alcohol 
• 127-68-4 sodium 3-nitrobenzenesulfonate 
• 51788-72-8 allyl (3,4-dimethylphenyl) ether 
• 91-66-7 N,N-diethylaniline 
• 95-65-8 3,4-Dimethylphenol 
• 67-66-3 chloroform 
• 50-00-0 formaldehyd 
• 5973-71-7 3,4-dimethylbenzaldehyde 
• 86582-31-2 2-methoxy-4,5-dimethylbenzaldehyde 
• 100-97-0 hexamethylenetetramine 
• 74-90-8 hydrogen cyanide 

Downstream Products

• 1315577-48-0 (E)-4,5-dimethyl-2-styrylphenol 
• 132675-12-8 2-[[4-(hydroxymethyl)piperidin-1-yl]methyl]-4,5-dimethylphenol 
• 3938-14-5 3-bromo-4,5-dimethylpyrocatechol 
• 91061-36-8 2-methoxy-4,5-dimethylbenzoic acid 
• 7771-25-7 2-methoxy-4,5-dimethylphenol 
• 95835-74-8 5,6-Dimethyl-benzofuran-2-carboxylic acid 
• 2785-74-2 4,5-dimethylbenzene-1,2-diol 
• 86582-31-2 2-methoxy-4,5-dimethylbenzaldehyde 

Relevant articles and documents

-

-

One-Pot Synthesis of Functionalized Fused Furans via a BODIPY-Catalyzed Domino Photooxygenation

Six-membered ring fused furans containing a tetrasubstituted tertiary carbon were prepared in an unprecedented one-pot BODIPY-catalyzed domino photooxygenation/reduction process. A series of functionalized furans was synthesized from readily available 2-alkenylphenols and mechanistic studies were performed to account for the domino photosensitized oxygenation.

BORONIC ACID BEARING LIPHAGANE COMPOUNDS AS INHIBITORS OF P13K- a AND/OR B

Compounds with unique liphagane meroterpenoid scaffold having boronic acid functionality in the skeleton are described (formula 1) together with pharmacological potential of these compounds as anticancer agents. A method of preparation and inhibiting the activity of phosphoinositide-3-kinase (PI3K-alpha and beta) has been presented. In particular, the invention describes a method of inhibiting PI3K isoforms, wherein the compounds are novel structures based on liphagane scaffold with unique boronic acid functionality. The methods and uses thereof are described herein this invention.