(2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone - >97.0%(GC), high purity , CAS No.346440-54-8

  • ≥97%(GC)
Item Number
S161185
Grouped product items
SKUSizeAvailabilityPrice Qty
S161185-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$109.90
S161185-250mg
250mg
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$178.90
S161185-1g
1g
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$583.90
S161185-5g
5g
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$2,334.90

Discover (2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone by Aladdin Scientific in >97.0%(GC) for only $109.90. Available - in Ligands at Aladdin Scientific. Tags: asymmetric synthesis, Chiral organic catalyst.

Basic Description

SynonymsQ27270710 | (2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone | T70804 | (2S,5S)-(-)-5-Benzyl-2-tert-butyl-3-methyl-4-imidazolidinone | J-019688 | AKOS000272101 | NSC 400336 | CS-0093648 | Macmillan's imidazolidinone catalysts second generation
Specifications & Purity≥97%(GC)
Shipped InNormal
Product Description

product description:

(2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone is a chiral imidazolidinone organocatalyst, developed by MacMillan and co-workers.


application:

(2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone is a second-generation MacMillan catalyst, which can be used as a chiral organocatalyst in:

The chiral transformation reaction, including Friedel-Crafts and Mukaiyama-Michael reactions.

The preparation of substituted spiroundecenetriones via asymmetric domino Knoevenagel/Diels-Alder reactions.

The asymmetric synthesis of β-hydroxy aldehydes and their dimethylacetals via aldehyde-aldehyde aldol condensation reaction.

The enantioselective α-fluorination of aldehydes using N-fluorobenzenesulfonamide as a fluorinating agent.

The stereoselective preparation of (oxomethyl)oxabicyclo[3.2.1]octenones and tricyclic pyrroles via [4+3] cycloaddition of (trialkylsiloxy)pentadienals to furans.

Metal-free OrganoCatalyst technology for asymmetric catalysis. Catalyzes asymmetric indole alkylations, Friedel-Crafts alkylations, and a broad range of conjugate addition reactions in high enantiomeric excess.

Names and Identifiers

IUPAC Name (2S,5S)-5-benzyl-2-tert-butyl-3-methylimidazolidin-4-one
INCHI InChI=1S/C15H22N2O/c1-15(2,3)14-16-12(13(18)17(14)4)10-11-8-6-5-7-9-11/h5-9,12,14,16H,10H2,1-4H3/t12-,14-/m0/s1
InChi Key SKHPYKHVYFTIOI-JSGCOSHPSA-N
Canonical SMILES CC(C)(C)C1NC(C(=O)N1C)CC2=CC=CC=C2
Isomeric SMILES CC(C)(C)[C@H]1N[C@H](C(=O)N1C)CC2=CC=CC=C2
WGK Germany 3
PubChem CID 10309834
Molecular Weight 246.35
Reaxy-Rn 6480916

Certificates

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Lot NumberCertificate TypeDateItem
E2421431Certificate of AnalysisMar 30, 2024 S161185

Chemical and Physical Properties

Specific Rotation[α]-60° (C=1,MeOH)
Melt Point(°C)100 °C

Safety and Hazards(GHS)

WGK Germany 3
Reaxy-Rn 6480916

Related Documents

Solution Calculators