84562-48-1

Basic information

• Product Name: 4-DIMETHYLAMINO-2-METHOXYBENZALDEHYDE
• Synonyms: 4-DIMETHYLAMINO-2-METHOXYBENZALDEHYDE;2-Methoxy-4-dimethylaminobenzaldehyde;NSC 156544
• CAS NO: 84562-48-1
• Molecular Formula: C₁₀H₁₃NO₂
• Molecular Weight: 179.22
• Product Categories: Aromatic Aldehydes & Derivatives (substituted)
• Mol File: 84562-48-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 58-60°C
• Boiling Point: 305.9 °C at 760 mmHg
• Flash Point: 138.8 °C
• Appearance: /
• Density: 1.098 g/cm³
• Vapor Pressure: 0.000796mmHg at 25°C
• Refractive Index: 1.576
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Solubility: Slightly soluble 0.32 g/L at 25°C.
• PKA: 1.34±0.22(Predicted)
• Sensitive: Air Sensitive
• BRN: 2719181
• CAS DataBase Reference: 4-DIMETHYLAMINO-2-METHOXYBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-DIMETHYLAMINO-2-METHOXYBENZALDEHYDE(84562-48-1)
• EPA Substance Registry System: 4-DIMETHYLAMINO-2-METHOXYBENZALDEHYDE(84562-48-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36-36/37
• Hazardous Substances Data: 84562-48-1(Hazardous Substances Data)

Usage

Uses

4-Dimethylamino-2-methoxybenzaldehyde is used to produce 2,6-Dichloro-N'-(4-dimethylamino-2-methoxy-benzylidene)-benzene-1,4-diamine.

InChI:InChI=1/C10H13NO2/c1-11(2)9-5-4-8(7-12)10(6-9)13-3/h4-7H,1-3H3

Upstream product

• 15799-79-8 3-methoxy-N,N-dimethylaniline 
• 68-12-2 N,N-dimethyl-formamide 
• 74-83-9 methyl bromide 
• 41602-56-6 4-dimethylamino-2-hydroxy-benzaldehyde 
• 450-83-9 4-fluoro-2-methoxybenzaldehyde 
• 124-40-3 dimethyl amine 

Downstream Products

• 84562-49-2 2,6-Dichloro-N'-[1-(4-dimethylamino-2-methoxy-phenyl)-meth-(E)-ylidene]-benzene-1,4-diamine 
• 1268353-54-3 C₂₄H₂₆N₆O₂ 
• 910813-79-5 3-(4-dimethylamino-2-methoxyphenyl)-1-((1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propan-1-one 
• 1254798-64-5 (Z)-5-bromo-4-chloro-2-(4-dimethylamino-2-methoxybenzylidene)indolin-3-one 

Relevant articles and documents

Evidence of acid mediated enhancement of photoinduced charge transfer reaction in 2-methoxy-4-(N,N-dimethylamino)benzaldehyde: Spectroscopic and quantum chemical study

The photophysical behavior of 2-methoxy-4-(N,N-dimethylamino)benzaldehyde (2-MDMABA) has been investigated by steady state absorption and emission spectroscopy, time resolved emission spectroscopy and quantum chemical calculations. The molecule 2-MDMABA h

Effect of phenyl ring substitution on J-aggregate formation ability of novel bisazomethine dyes in vapour-deposited films

Bisazomethine dyes, which are synthesized using diaminomaleonitrile and aminobenzaldehydes, exhibit red fluorescence in solution and in the solid state. Several bisazomethine dyes are known to form J-aggregates in vapour-deposited films. In this work, novel bisazomethine dyes were synthesized and the effect of phenyl ring substitution on the J-aggregate formation in vapour-deposited films was examined. The optical properties of the dyes were examined in solution and in the solid state through molecular orbital calculations. Four derivatives were found to form J-aggregates in vapour-deposited films as determined from the shape of the spectrum and the absorption edge.

N2-(4-Substituted-2,6-dichlorophenyl)-N1,N1-dimethylformamidines as Antihypertensive and Diuretic Agents

The synthesis of a series of N2--2,6-dichlorophenyl>-N1,N1-dimethylformamidines that caused marked blood pressure lowering and/or diuresis in spontaneously hypertensive rats (SHR) is reported.Diuretic activity was not always associated with acute antihypertensive activity.Central nervous system effects, most notably sedation, were observed.Compound 9d, which lowered arterial blood pressure 37 mmHg in SHR when dosed at 100 mg/kg, was further evaluated in chronic hypertensive dogs because of apparent minimal CNS effects.A reduction in arterial blood pressure of 32 mmHg at 1.0 mg/kg during a 6-h postdosing interval was observed.This response was unrelated to α- or β-adrenergic blockade, angiotensin I antagonism, or neuronal or ganglionic blockade.CNS effects were also observed.