480424-73-5

Basic information

• Product Name: (5R)-(HYDROXYMETHYL-3-((1R)-1-PHENYLETH&
• Synonyms: (5R)-(HYDROXYMETHYL-3-((1R)-1-PHENYLETH&;3-(1'(R)-ALPHA-METHYLBENZYL)-5(R)-HYDRO&;(5r)-(hydroxymethyl-3-[(1r)-1-phenylethyl]-2-oxazolidinone;(r)-5-(hydroxymethyl)-3-[(r)-α-methylbenzyl-2-oxazolidinone;3-(1μ-(R)-α-Methylbenzyl)-5(R)-hydroxymethyl-oxazolidin-2-one, (R)-5-(Hydroxymethyl)-3-[(R)-α-methylbenzyl-2-oxazolidinone;(5R)-Hydroxymethyl-3-[(1R)-phenylethyl]-oxazolidin-2-one;(R)-rel-5-(Hydroxymethyl)-3-((R)-1-phenylethyl)oxazolidin-2-one;(5R)-5-(hydroxymethyl)-3-[(1R)-1-phenylethyl]-1,3-oxazolidin-2-one
• CAS NO: 480424-73-5
• Molecular Formula: C12H15NO3
• Molecular Weight: 221.255
• Mol File: 480424-73-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 100-105 °C(lit.)
• Boiling Point: 444.4°C at 760 mmHg
• Flash Point: 222.6°C
• Appearance: /
• Density: 1.219g/cm³
• Vapor Pressure: 1.12E-08mmHg at 25°C
• Refractive Index: 1.565
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: (5R)-(HYDROXYMETHYL-3-((1R)-1-PHENYLETH&(CAS DataBase Reference)
• NIST Chemistry Reference: (5R)-(HYDROXYMETHYL-3-((1R)-1-PHENYLETH&(480424-73-5)
• EPA Substance Registry System: (5R)-(HYDROXYMETHYL-3-((1R)-1-PHENYLETH&(480424-73-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 480424-73-5(Hazardous Substances Data)

Usage

General Description

The chemical compound "(5R)-(HYDROXYMETHYL-3-((1R)-1-PHENYLETH" is a stereoisomer of a compound with a hydroxymethyl group attached to a phenylethyl molecule. The "5R" designation indicates the absolute stereochemistry of the compound, while the "1R" designation indicates the stereochemistry of the phenylethyl group. (5R)-(HYDROXYMETHYL-3-((1R)-1-PHENYLETH& likely has potential applications in organic synthesis, medicinal chemistry, or materials science due to its unique stereochemistry and functional groups. Further research and characterization of this compound may reveal its specific properties and potential uses in various fields.

InChI:InChI=1/C12H15NO3/c1-9(10-5-3-2-4-6-10)13-7-11(8-14)16-12(13)15/h2-6,9,11,14H,7-8H2,1H3/t9-,11-/m1/s1

Upstream product

• 113420-84-1 (1'S^*,5R^*)-3-(1'-phenyleth-1'-yl)-5-(acetoxymethyl)oxazolidin-2-one 
• 113420-78-3 (1'S^*,5S^*)-3-(1'-phenyleth-1'-yl)-5-(acetoxymethyl)oxazolidin-2-one 
• 113420-77-2 (1'S^*,5S^*)-3-(1'-phenyleth-1'yl)-5-(iodomethyl)oxazolidin-2-one 
• 113420-76-1 (S)-N-(1-phenyleth-1-yl)-N-(prop-2-en-1-yl)amine hydrobromide 
• 113471-09-3 (S)-N-(1-phenyleth-1-yl)-N-(prop-2-en-1-yl)-N-(benzyloxycarbonyl)amine 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 595549-63-6 (5R)-3-[(1S)-1-phenylethyl]-5-vinyl-1,3-oxazolidin-2-one 
• 113420-83-0 (1'S^*,5R^*)-3-(1'-phenyleth-1'yl)-5-(iodomethyl)oxazolidin-2-one 

Downstream Products

• 637343-57-8 (5R)-Azidomethyl-3-[(1R)-phenylethyl-oxazolidine-2-one] 

Relevant articles and documents

A simple and easy access to 3-N-alkyl-5-vinyloxazolidinones mediated by palladium-phosphine catalysts

A new entry for the synthesis of 3-alkyl substituted 5-vinyloxazolidin-2-one derivatives 2 from cis-2-butenylene-1,4-dicarbonate 1 and primary amines mediated by palladium-phosphine catalysts is described. The scope and limitation, a plausible mechanism, and an asymmetric version of the reaction are also discussed.