73096-98-7

Basic information

• Product Name: 1-{3-[(dimethylamino)methyl]-4-hydroxyphenyl}ethanone
• Synonyms: 1-[3-[(Dimethylamino)methyl]-4-hydroxyphenyl]ethanone; 1-{3-[(Dimethylamino)methyl]-4-hydroxyphenyl}ethanone; 1VR DQ C1N1& 1; 430-920-1; 73096-98-7; Ethanone, 1-[3-[(dimethylamino)methyl]-4-hydroxyphenyl]-
• CAS NO: 73096-98-7
• Molecular Formula: C₁₁H₁₅NO₂
• Molecular Weight: 193.2423
• EINECS: 430-920-1
• Mol File: 73096-98-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 328.7°C at 760 mmHg
• Flash Point: 152.6°C
• Density: 1.098g/cm³
• Vapor Pressure: 9.73E-05mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: 1-{3-[(dimethylamino)methyl]-4-hydroxyphenyl}ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{3-[(dimethylamino)methyl]-4-hydroxyphenyl}ethanone(73096-98-7)
• EPA Substance Registry System: 1-{3-[(dimethylamino)methyl]-4-hydroxyphenyl}ethanone(73096-98-7)

Safety Data

• Hazardous Substances Data: 73096-98-7(Hazardous Substances Data)

Usage

Appearance

Yellow crystalline solid

Usage

Commonly used in the synthesis of pharmaceuticals and organic compounds

Potential applications

Studied for its potential applications in the field of photochemistry and photophysics

Chemical groups

Contains a hydroxy group and a dimethylamino group

Versatility

Acts as a versatile building block for the synthesis of various organic molecules with potential biological and chemical properties

Derivative

A derivative of acetophenone

Upstream product

• 24085-05-0 1-(3-chloromethyl-4-hydroxyphenyl)ethanone 
• 124-40-3 dimethyl amine 
• 50-00-0 formaldehyd 
• 99-93-4 4-Hydroxyacetophenone 
• 33797-51-2 eschenmoser's salt 
• 36627-00-6 N,N-dimethylaminomethyl iodide 

Downstream Products

• 93344-83-3 Thiophosphoric acid O-(4-acetyl-2-dimethylaminomethyl-phenyl) ester O',O''-diethyl ester 
• 24085-06-1 4'-acetoxy-3'-(acetoxymethyl)acetophenone 
• 1594133-58-0 (E)-3-(6-chloro-7-fluoro-4-morpholinoquinolin-2-yl)-1-(3-((dimethylamino)methyl)-4-hydroxyphenyl)prop-2-en-1-one 
• 1594133-59-1 (E)-3-(6-chloro-7-fluoro-4-(4-fluorophenyl) quinolin-2-yl)-1-(3-((dimethylamino)methyl)-4-hydroxyphenyl)prop-2-en-1-one 
• 1594133-60-4 (E)-3-(6-chloro-4-(4-methoxyphenyl) quinolin-2-yl)-1-(3-((dimethylamino) methyl)-4-hydroxy phenyl)prop-2-en-1-one 
• 1594133-63-7 (E)-3-(6-chloro-4-(4-fluorophenyl) quinolin-2-yl)-1-(3-((dimethylamino) methyl)-4-hydroxyphenyl) prop-2-en-1-one 

Relevant articles and documents

Synthesis of the β2 Agonist (R)-Salmeterol Using a Sequence of Supported Reagents and Scavenging Agents

(Matrix Presented) The enantioselective synthesis of (R)-salmeterol has been achieved by using a sequence of supported reagents and sequestering agents. The saligenin core was installed by a regiospecific alkylation and a chiral auxiliary approach was employed to introduce the desired stereochemistry via a diastereoselective reduction.

Synthesis and Insecticidal Activity of Some New 3-Substituted 4-Hydroxyacetophenones

A number of 3-(N,N-dialkylaminomethyl)-4-hydroxy acetophenones (4-10) and their thiophosphorylated compounds (11-16) have been synthesised and screened for their insecticidal activity.Only thiophosphorylated compounds are found to possess significant activity.The intramolecular hydrogen bonding in these compounds has also been discussed.