29194-04-5

Basic information

• Product Name: 2-(benzyl(methyl)amino)-1-phenylethanol
• Synonyms: 2-(benzyl(methyl)amino)-1-phenylethanol
• CAS NO: 29194-04-5
• Molecular Formula: C₁₆H₁₉NO
• Molecular Weight: 241.32816
• Mol File: 29194-04-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 378.248 °C at 760 mmHg
• Flash Point: 142 °C
• Appearance: /
• Density: 1.09 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.591
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 13.94±0.20(Predicted)
• CAS DataBase Reference: 2-(benzyl(methyl)amino)-1-phenylethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(benzyl(methyl)amino)-1-phenylethanol(29194-04-5)
• EPA Substance Registry System: 2-(benzyl(methyl)amino)-1-phenylethanol(29194-04-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 29194-04-5(Hazardous Substances Data)

Usage

General Description

2-(benzyl(methyl)amino)-1-phenylethanol is a chemical compound with the molecular formula C16H19NO. It is a tertiary amine and alcohol derivative with a benzyl group, a methyl group, and a phenyl group attached to the nitrogen and carbon atoms, respectively. 2-(benzyl(methyl)amino)-1-phenylethanol is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It has potential applications in medicinal chemistry and drug development due to its pharmacological and biological properties. 2-(benzyl(methyl)amino)-1-phenylethanol is also used in research and laboratory settings as a reagent and building block for the synthesis of complex organic molecules. Overall, this chemical compound has versatile uses and is an important ingredient in the production of various compounds in the pharmaceutical and chemical industries.

InChI:InChI=1/C16H19NO/c1-17(12-14-8-4-2-5-9-14)13-16(18)15-10-6-3-7-11-15/h2-11,16,18H,12-13H2,1H3

Upstream product

• 114751-41-6 2-(benzyl(methyl)amino)-1phenylethanone hydrochloride 
• 108-86-1 bromobenzene 
• 88953-56-4 3-methyl-5-phenyloxazolidine 
• 93-56-1 phenylethane 1,2-diol 
• 103-67-3 benzyl-methyl-amine 
• 1147090-56-9 2-(N-benzyl-N-methylamino)-1-phenylethyl N',N'-diisopropylcarbamate 
• 100-52-7 benzaldehyde 
• 70-11-1 α-bromoacetophenone 
• 33350-26-4 2-(N-benzyl-N-methylamino)acetophenone 
• 96-09-3 styrene oxide 

Downstream Products

• 83657-22-1 uniconazole 
• 25771-97-5 2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 33350-26-4 2-(N-benzyl-N-methylamino)acetophenone 
• 87098-81-5 (R)-N-benzyl-N-methyl-β-hydroxyphenethylamine 
• 101436-25-3 N-Methyl-N-benzyl-2-brom-2-phenyl-aethylamin 
• 102560-83-8 1-benzoyloxy-2-(benzyl-methyl-amino)-1-phenyl-ethane 

Relevant articles and documents

Method for Ir/f-amphox high-efficiency synthesis of chiral α- C-amino alcohol by virtue of catalytic oxidation 1,2- of P-aminoketone by using one-aminoketone

The invention discloses a method for efficiently synthesizing chiral 1,2-amino alcohol by catalyzing alpha-aminoketone through Ir/f-amphox. A ligand f-amphox used by the method can be more easily synthesized; the reaction has the characteristics of enanti

4-Phenyl tetrahydroisoquinolines as dual norepinephrine and dopamine reuptake inhibitors

Novel 4-phenyl tetrahydroisoquinolines that inhibit both dopamine and norepinephrine transporters were designed and prepared. In this Letter, we describe the synthesis, in vitro activity and associated structure-activity relationships of this series. We also report the ex vivo NET occupancy of a representative compound, 41.

Direct syntheses of 4-aryl-1,2,3,4-tetrahydroisoquinolines and 1-aryl-2,3,4,5-tetrahydro-3-benzoazepines via hydroamination of enol carbamates

An efficient and simple procedure for the syntheses of 4-aryl-1,2,3,4-tetrahydroisoquinolines and 1-aryl-2,3,4,5-tetrahydro-3-benzoazepines has been developed. The approach uses easily available starting materials and requires just three steps. The hydroamination of an enol carbamate is the key step. This general and direct method has been applied to the total synthesis of the natural alkaloid cherylline and to biologically active 3-benzoazepines as well.