(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% CAS 415678-40-9

Introduction:Basic information about (2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% CAS 415678-40-9, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(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...;)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone;(2S,5S)-(–(2S,5S)-(–)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone
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% 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℃
storage temp. Storage temp. 2-8°C
pka4.44±0.60(Predicted)
AppearanceLight yellow to yellow Liquid
InChI1S/C16H18N2O2/c1-11-8-9-14(20-11)15-17-13(16(19)18(15)2)10-12-6-4-3-5-7-12/h3-9,13,15,17H,10H2,1-2H3/t13-,15-/m0/s1
InChIKeyIQIMPHPFMHVWBZ-ZFWWWQNUSA-N
SMILESCN1[C@H](N[C@@H](Cc2ccccc2)C1=O)c3ccc(C)o3

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
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

(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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