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16251-46-0

  • Product Nameephedroxane
  • Molecular FormulaC11H13 N O2
  • Molecular Weight191.23
  • Purity99%
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Product Details

Quick Details

  • CasNo： 16251-46-0
  • Molecular Formula： C11H13 N O2
  • Purity： 99%

Reputable manufacturer supply ephedroxane 16251-46-0 in stock with high standard

  • Molecular Formula:C11H13 N O2
  • Molecular Weight:191.23
  • Vapor Pressure:1.12E-05mmHg at 25°C 
  • Boiling Point:370.3°Cat760mmHg 
  • Flash Point:177.8°C 
  • PSA：29.54000 
  • Density:1.115g/cm3 
  • LogP:2.13610 

ephedroxane(Cas 16251-46-0) Usage

InChI:InChI=1/C11H13NO2/c1-8-10(14-11(13)12(8)2)9-6-4-3-5-7-9/h3-8,10H,1-2H3/t8-,10-/m0/s1

16251-46-0 Relevant articles

Pure by NMR ?

Claridge, Timothy D. W.,Davies, Stephen G.,Polywka, Mario E. C.,Roberts, Paul M.,Russell, Angela J.,Savory, Edward D.,Smith, Andrew D.

, p. 5433 - 5436 (2008)

(Chemical Equation Presented) Integratio...

Synthesis of 2-Arylethylamines by the Curtius Rearrangement

Schulze, Matthias

experimental part, p. 1461 - 1476 (2010/07/08)

2-Arylethylamine derivatives were synthe...

Carbon dioxide as a carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas: Scope and limitations

Paz, Jairo,Perez-Balado, Carlos,Iglesias, Beatriz,Munoz, Luis

supporting information; experimental part, p. 3037 - 3046 (2010/07/15)

Carbon dioxide can be used as a convenie...

1,3-Heterazolidines-2-heterounsaturated compounds derived from ephedrines

Cruz, Alejandro,Contreras, Rosalinda,Padilla-Martinez, Itzia I.,Juarez-Juarez, Minerva

, p. 1499 - 1505 (2007/10/03)

Herein, a direct and easy method for pre...

16251-46-0 Process route

4-methyl-5-phenyl-2-oxazolidinone
54418-69-8

4-methyl-5-phenyl-2-oxazolidinone

methyl iodide
74-88-4

methyl iodide

trans-3,4-dimethyl-5-phenyloxazolidin-2-one
6317-31-3,15833-15-5,16251-46-0,16251-47-1,32461-36-2,32461-37-3,91049-48-8,91049-51-3,91740-65-7

trans-3,4-dimethyl-5-phenyloxazolidin-2-one

(4RS,5SR)-3,4-dimethyl-5-phenyloxazolidin-2-one
6317-31-3,15833-15-5,16251-46-0,16251-47-1,32461-36-2,32461-37-3,91049-48-8,91049-51-3,91740-65-7

(4RS,5SR)-3,4-dimethyl-5-phenyloxazolidin-2-one

Conditions
Conditions Yield
4-methyl-5-phenyl-2-oxazolidinone; With potassium tert-butylate; In tetrahydrofuran; for 0.25h; Cooling with ice;
methyl iodide; In tetrahydrofuran; at 20 ℃; Cooling with ice;
4-methyl-5-phenyl-2-oxazolidinone
54418-69-8

4-methyl-5-phenyl-2-oxazolidinone

methyl iodide
74-88-4

methyl iodide

trans-3,4-dimethyl-5-phenyloxazolidin-2-one
6317-31-3,15833-15-5,16251-46-0,16251-47-1,32461-36-2,32461-37-3,91049-48-8,91049-51-3,91740-65-7

trans-3,4-dimethyl-5-phenyloxazolidin-2-one

(4RS,5SR)-3,4-dimethyl-5-phenyloxazolidin-2-one
6317-31-3,15833-15-5,16251-46-0,16251-47-1,32461-36-2,32461-37-3,91049-48-8,91049-51-3,91740-65-7

(4RS,5SR)-3,4-dimethyl-5-phenyloxazolidin-2-one

Conditions
Conditions Yield
4-methyl-5-phenyl-2-oxazolidinone; With potassium tert-butylate; In tetrahydrofuran; for 0.25h; Cooling with ice;
methyl iodide; In tetrahydrofuran; at 20 ℃; Cooling with ice;

16251-46-0 Upstream products

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16251-46-0 Downstream products

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    1201-56-5

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