15182-06-6

Basic information

• Product Name: 2-[2-(DIMETHYLAMINO)ETHOXY]BENZALDEHYDE 97
• Synonyms: 2-[2-(DIMETHYLAMINO)ETHOXY]BENZALDEHYDE 97;2-[2-(Dimethylamino)ethoxy]benzaldehyde 97%;2-[2-(dimethylamino)ethoxy]benzaldehyde(SALTDATA: HCl);2-[2-(dimethylamino)ethoxy]benzaldehyde 1HCl;N,N-Dimethyl-2-(2-formylphenoxy)ethylamine
• CAS NO: 15182-06-6
• Molecular Formula: C₁₁H₁₅NO₂
• Molecular Weight: 193.2445
• Mol File: 15182-06-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 303.6°Cat760mmHg
• Flash Point: 137.4°C
• Appearance: /
• Density: 1.062g/cm³
• Vapor Pressure: 0.000922mmHg at 25°C
• Refractive Index: 1.542
• PKA: 8.61±0.28(Predicted)
• CAS DataBase Reference: 2-[2-(DIMETHYLAMINO)ETHOXY]BENZALDEHYDE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-(DIMETHYLAMINO)ETHOXY]BENZALDEHYDE 97(15182-06-6)
• EPA Substance Registry System: 2-[2-(DIMETHYLAMINO)ETHOXY]BENZALDEHYDE 97(15182-06-6)

Safety Data

• Hazard Codes: C
• Hazardous Substances Data: 15182-06-6(Hazardous Substances Data)

Usage

General Description

2-[2-(Dimethylamino)ethoxy]benzaldehyde 97 is a chemical compound with a complex structure. The compound's formula contains elements such as carbon, hydrogen, nitrogen, and oxygen. It is characterized by the presence of a benzaldehyde group, which is a type of aromatic aldehyde, and an ethoxy group, a functional group consisting of an ether linked to an ethanol. Additionally, 2-[2-(Dimethylamino)ethoxy]benzaldehyde 97 contains a dimethylamino group, which involves two methyl groups attached to an amino group. This chemical can be utilized in various applications due to its properties, but specific uses depend on the context and combinations with other substances.

InChI:InChI=1/C11H15NO2/c1-12(2)7-8-14-11-6-4-3-5-10(11)9-13/h3-6,9H,7-8H2,1-2H3

Upstream product

• 90-02-8 salicylaldehyde 
• 107-99-3 2-(dimethylamino)ethyl chloride 
• 108-95-2 phenol 
• 4584-46-7 (2-chloroethyl)dimethylamine hydrochloride 
• 54373-14-7 2-(2-chloroethoxy)benzoic aldehyde 
• 124-40-3 dimethyl amine 
• 106-93-4 ethylene dibromide 
• 6052-79-5 2-(2-hydroxyphenyl)-1,3-dioxane 
• 1391906-41-4 2-(dimethylamino)ethyl ethyl carbonate 
• 13468-02-5 dimethyl(2-phenoxyethyl)amine 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 88159-72-2 (E)-3-[2-(2-Dimethylamino-ethoxy)-phenyl]-2-thiophen-2-yl-acrylonitrile; hydrochloride 
• 88136-98-5 (Z)-3-[2-(2-Dimethylamino-ethoxy)-phenyl]-2-(1H-indol-3-yl)-acrylonitrile 
• 86759-03-7 [4-(10,11-Dihydro-dibenzo[b,f]thiepin-10-yl)-piperazin-1-yl]-[1-[2-(2-dimethylamino-ethoxy)-phenyl]-meth-(E)-ylidene]-amine 
• 84203-09-8 2-(2-(4,5-diphenyl-1H-imidazol-2-yl)phenoxy)-N,N-dimethylethanamine 
• 1301625-97-7 C₁₆H₂₇N₃O 
• 1301625-95-5 C₁₅H₂₅N₃O 
• 112562-93-3 2-[2-(2-Dimethylamino-ethoxy)-phenyl]-thiazolidine-3-carbothioic acid methylamide; hydrochloride 
• 86759-05-9 [4-(8-Chloro-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazin-1-yl]-[1-[2-(2-dimethylamino-ethoxy)-phenyl]-meth-(E)-ylidene]-amine 
• 114896-52-5 1-(2-(2-dimethylaminoethoxy)phenyl)-2,3,4,9-tetrahydro-1H-pyrido<3,4-b>indole hydrochloride 
• 91215-97-3 2-(2-dimethylamino-ethoxy)-benzylamine 

Relevant articles and documents

Mustard Carbonate Analogues as Sustainable Reagents for the Aminoalkylation of Phenols

N,N-dialkyl ethylamine moiety can be found in numerous scaffolds of macromolecules, catalysts, and especially pharmaceuticals. Common synthetic procedures for its incorporation in a substrate relies on the use of a nitrogen mustard gas or on multistep syntheses featuring chlorine hazardous/toxic chemistry. Reported herein is a one-pot synthetic approach for the easy introduction of aminoalkyl chain into different phenolic substrates through dialkyl carbonate (β-aminocarbonate) chemistry. This new direct alcohol substitution avoids the use of chlorine chemistry, and it is efficient on numerous pharmacophore scaffolds with good to quantitative yield. The cytotoxicity via MTT of the β-aminocarbonate, key intermediate of this synthetic approach, was also evaluated and compared with its alcohol precursor.

Synthesis, cytotoxicity and topoisomerase inhibition properties of multifarious aminoalkylated indeno[1,2-c]isoquinolin-5,11-diones

A number of mono- or diaminoalkylated indeno[1,2-c]isoquinolin-5,11-diones analogs of 1 were synthesized and evaluated for their DNA binding affinities, topoisomerase inhibition properties and antiproliferative activities against human cancer cell lines (

Diphenyl-substituted heterocycles, processes for preparing them and their use as pharmaceutical compositions

The invention relates to new diphenyl-substituted 5-ring heterocycles of general formula (I) wherein A, X and the groups R1, R2, R3, R4and R5are defined as in the claims, processes for preparing them