58997-89-0

Basic information

• Product Name: 2-(dimethylamino)-2-phenylbutyl (+-)-3,4,5-trimethoxybenzoate
• Synonyms: 2-(Dimethylamino)-2-phenylbutyl (.+.-)-3,4,5-trimethoxybenzoate; 2-phenylbutyl 2-(dimethylamino)-3,4,5-trimethoxybenzoate
• CAS NO: 58997-89-0
• Molecular Formula: C₂₂H₂₉NO₅
• Molecular Weight: 387.4694
• EINECS: 261-546-5；261-547-0
• Mol File: 58997-89-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 502.7°C at 760 mmHg
• Flash Point: 257.8°C
• Density: 1.112g/cm³
• Vapor Pressure: 3.11E-10mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: 2-(dimethylamino)-2-phenylbutyl (+-)-3,4,5-trimethoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(dimethylamino)-2-phenylbutyl (+-)-3,4,5-trimethoxybenzoate(58997-89-0)
• EPA Substance Registry System: 2-(dimethylamino)-2-phenylbutyl (+-)-3,4,5-trimethoxybenzoate(58997-89-0)

Safety Data

• Hazardous Substances Data: 58997-89-0(Hazardous Substances Data)

Usage

General Description

The chemical 2-(dimethylamino)-2-phenylbutyl (+-)-3,4,5-trimethoxybenzoate is a synthetic compound that has a combination of a dimethylamino group, a phenyl group, and a butyl group linked to a 3,4,5-trimethoxybenzoate. This chemical can have potential applications in the pharmaceutical industry due to its structural features, which may make it suitable for use as a drug or medication. The precise function and properties of this compound may vary depending on the specific stereochemistry of the molecule. Further research and testing would be necessary to fully understand the potential uses and impacts of this chemical.

Upstream product

• 557-04-0 magnesium stearate 

Downstream Products

• 3840-31-1 (3,4,5-trimethoxyphenyl)methanol 
• 39068-94-5 2-phenyl-2-dimethylamino-1-butanol 
• 1456509-28-6 trimebutine methanesulfonic acid salt 
• 1456509-48-0 trimebutine 4-thiocarbamoylbenzenesulfonate 
• 1456509-46-8 trimebutine 3-thiocarbamoylbenzenesulfonate 
• 1456509-49-1 trimebutine 4-toluenesulfonate 
• 1456509-35-5 trimebutine 3-sulfobenzoic acid salt 

Relevant articles and documents

Direct Conversion of N-Alkylamines to N-Propargylamines through C-H Activation Promoted by Lewis Acid/Organocopper Catalysis: Application to Late-Stage Functionalization of Bioactive Molecules

An efficient catalytic method to convert an α-C-H bond of N-alkylamines into an α-C-alkynyl bond was developed. In the past, such transformations were carried out under oxidative conditions, and the enantioselective variants were confined to tetrahydroisoquinoline derivatives. Here, we disclose a method for the union of N-alkylamines and trimethylsilyl alkynes, without the presence of an external oxidant and promoted through cooperative actions of two Lewis acids, B(C6F5)3 and a Cu-based complex. A variety of propargylamines can be synthesized in high diastereo-and enantioselectivity. The utility of the approach is demonstrated by the late-stage site-selective modification of bioactive amines. Kinetic investigations that shed light on various mechanistic nuances of the catalytic process are presented.