ChemicalBook > Product Catalog > Organic Chemistry > Heterocyclic Compounds > (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%
(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
- Mol File:
- 415678-40-9.mol
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(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
- Flash point:
- >110℃
- storage temp.
- Storage temp. 2-8°C
- pka
- 4.44±0.60(Predicted)
- Appearance
- Light yellow to yellow Liquid
- InChI
- 1S/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
- InChIKey
- IQIMPHPFMHVWBZ-ZFWWWQNUSA-N
- SMILES
- CN1[C@H](N[C@@H](Cc2ccccc2)C1=O)c3ccc(C)o3
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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 Class
- 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects - Hazard Classifications
- Acute Tox. 3 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
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(2S,5S)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone, 95% Usage And Synthesis
Uses
Catalyst 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%Supplier
SynAsst Chemical.
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- 021-60343070
Sigma-Aldrich
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