55586-68-0

Basic information

• Product Name: 4-DIETHYLAMINO-2-METHOXY-BENZALDEHYDE
• Synonyms: 4-DIETHYLAMINO-2-METHOXY-BENZALDEHYDE;TIMTEC-BB SBB011177;2-Methoxy-4-(diethylamino)benzaldehyde;5-(Diethylamino)-2-formylanisole, N,N-Diethyl-4-formyl-3-methoxyaniline;Benzaldehyde, 4-(diethylamino)-2-methoxy-
• CAS NO: 55586-68-0
• Molecular Formula: C₁₂H₁₇NO₂
• Molecular Weight: 207.27
• Mol File: 55586-68-0.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 334.8°Cat760mmHg
• Flash Point: 156.3°C
• Appearance: /
• Density: 1.056g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.558
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-DIETHYLAMINO-2-METHOXY-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-DIETHYLAMINO-2-METHOXY-BENZALDEHYDE(55586-68-0)
• EPA Substance Registry System: 4-DIETHYLAMINO-2-METHOXY-BENZALDEHYDE(55586-68-0)

Safety Data

• Hazard Codes: Xi,T
• Statements: 25
• Safety Statements: 45
• HazardClass: IRRITANT
• Hazardous Substances Data: 55586-68-0(Hazardous Substances Data)

Usage

General Description

4-DIETHYLAMINO-2-METHOXY-BENZALDEHYDE, also known as 3-(diethylamino)-2-methoxybenzaldehyde, is a chemical compound with the molecular formula C11H15NO2. It is a colorless to yellow liquid with a pleasant floral scent. 4-DIETHYLAMINO-2-METHOXY-BENZALDEHYDE is commonly used as a reagent in organic synthesis and as a building block in the production of pharmaceuticals and fragrances. Additionally, it is utilized in the manufacturing of dyes and pigments. Its unique structure and properties make it a valuable compound in various industries and research applications.

InChI:InChI=1/C12H17NO2/c1-4-13(5-2)11-7-6-10(9-14)12(8-11)15-3/h6-9H,4-5H2,1-3H3

Upstream product

• 74-83-9 methyl bromide 
• 17754-90-4 4-(Diethylamino)salicylaldehyde 
• 450-83-9 4-fluoro-2-methoxybenzaldehyde 
• 109-89-7 diethylamine 
• 74-88-4 methyl iodide 

Downstream Products

• 753006-62-1 1-(4-diethylamino-2-methoxyphenyl)ethanol 
• 1268353-63-4 C₂₈H₃₄N₆O₂ 

Relevant articles and documents

Triphenylamine derived coumarin chalcones and their red emitting OBO difluoride complexes: Synthesis, photophysical and NLO property study

The auxiliary methoxy aided triphenylamine donors derived coumarin chalcones and their OBO complexes with branched donor-pi-acceptor systems are synthesized and characterized. Their photophysical properties are extensively studied in solvents of different polarity. They show strong emission solvatochromism and have quantum yields up to 0.87. The BF2-complexation of coumarin chalcones enhanced the quantum efficiency by approximately 1.4 times compared to the uncomplexed chalcones. Frontier molecular orbital analysis and Generalised Mulliken Hush analysis revealed a strong intramolecular charge transfer character of these chromophores. The first, second and third order polarizability of these chromophores are evaluated by the solvatochromic method and supported by Density Functional Theory calculations using CAM-B3LYP/6-31g(d) method. The third order nonlinear optical susceptibilities of these chromophores obtained by Z-scan analysis showed very less values of the imaginary part. Replacement of N-ethyl donors by aryl amine groups provided branched push-pull systems with enhanced thermal stability and nonlinear optical response.

A novel mitochondria-targeted ratiometric fluorescent probe for endogenous sulfur dioxide derivatives as a cancer-detecting tool

A new mitochondria-targeted fluorescent probe RBC, constructed using a coumarin moiety which was selected as the donor and a benzothiazole derivative as the acceptor, for SO2 derivatives (HSO3-/SO32-) was presented. The probe designed on a new FRET platform showed high selectivity and a low detection limit. Importantly, the probe could respond to HSO3-/SO32- within 35 s. Furthermore, the probe could target mitochondria and was successfully used for fluorescence imaging of endogenous bisulfite in HepG2 with low cytotoxicity, which significantly assisted in cancer diagnosis. This journal is

PHOTOINDUCED ELECTRON TRANSFER VOLTAGE-SENSITIVE COMPOUNDS

The disclosure provides methods to synthesize photoinduced electron transfer voltage-sensitive compounds, the compounds made therefrom, and uses of the compounds thereof.