6323-90-6

Basic information

• Product Name: 2-[(2-hydroxyethyl)amino]-1,2-diphenylethanone
• CAS NO: 6323-90-6
• Molecular Formula: C₁₆H₁₇NO₂
• Molecular Weight: 255.3117
• Mol File: 6323-90-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 440.7°C at 760 mmHg
• Flash Point: 220.4°C
• Density: 1.151g/cm³
• Vapor Pressure: 1.52E-08mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: 2-[(2-hydroxyethyl)amino]-1,2-diphenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2-hydroxyethyl)amino]-1,2-diphenylethanone(6323-90-6)
• EPA Substance Registry System: 2-[(2-hydroxyethyl)amino]-1,2-diphenylethanone(6323-90-6)

Safety Data

• Hazardous Substances Data: 6323-90-6(Hazardous Substances Data)

Usage

Usage

Precursor for the synthesis of various drugs in the pharmaceutical industry

Application

Research chemical in the study of organic chemistry and medicinal chemistry

Functional group

Hydroxyethylamine, useful for forming complex molecules and potential biological activity

Safety

Handle with caution and in accordance with proper safety protocols due to potential health hazards.

Relevant articles and documents

Substituted dialkanolamines, sulfur analogs and condensed 1,4-oxazine derivatives thereof in viral disease treatment

Substituted dialkanolamines, oxazine and sulfur analogs thereof, useful in treating shipping fever syndrome in mammals are disclosed having the formula: STR1 wherein: Ar is STR2 Z is oxygen or sulfur; R is selected from hydrogen, loweralkyl or STR3 R1 R2, R3, R4, R5, R6 and R7 are selected from hydrogen or loweralkyl; and STR4 when taken together may form a lowercycloalkyl ring or R5 with --ZR2 when taken together may form a 5-membered saturated oxygen or sulfur containing heterocyclic ring; X is selected from hydrogen, halo, loweralkoxy, loweralkyl, trifluoromethyl or dimethylamino and when X is more than 1, it may be the same radical or different; y is 0, 1 or 2; n is one, or zero and when n is 1, the stereoisomers thereof and when n is zero the dotted line becomes an oxygen-carbon bond forming an oxazine ring and the pharmaceutically acceptable acid addition salts thereof.