(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95%

(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% Basic information
Product Name:(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95%
Synonyms:(2s,5s)-5-benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidone;(2S,5S)-5-Benzyl-3-Methyl-2-(5-Methylfuran-2-yl)iMidazolidin-4-one;(2S,5S)-(-)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone 95%;4-Imidazolidinone, 3-methyl-2-(5-methyl-2-furanyl)-5-(phenylmethyl)-, (2S,5S)-;(2S,5S)-(-)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazo...
CAS:415678-40-9
MF:C16H18N2O2
MW:270.33
EINECS:
Product Categories:
Mol File:415678-40-9.mol
(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% Structure
(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% Chemical Properties
Boiling point 438.6±45.0 °C(Predicted)
density 1.155±0.06 g/cm3(Predicted)
refractive index n20/D1.5598
Fp >110℃
pka4.44±0.60(Predicted)
Safety Information
Hazard Codes T
Risk Statements 25-36/37/38
Safety Statements 26-36-45
RIDADR UN 2810 6.1 / PGIII
WGK Germany 3
MSDS Information
(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% Usage And Synthesis
UsesCatalyst for:
  • Enantioselective organocatalytic transfer hydrogenation of cycloalkenones with tert-Bu Hantzsch ester as source of hydrogen
  • Alkylation of indoles with an α,β-disubstituted α,β-unsaturated aldehyde in the enantioselective preparation of a selective serotonin reuptake inhibitor
  • MacMillan reaction
(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% Preparation Products And Raw materials

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