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795151

Sigma-Aldrich

(S)-t-Bu-Quinox

97%

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Synonym(s):
2-[(4S)-4-(1,1-dimethylethyl)-4,5-dihydro-2-oxazolyl]quinoline
Empirical Formula (Hill Notation):
C16H18N2O
CAS Number:
226387-12-8
Molecular Weight:
254.33
UNSPSC Code:
12352000
PubChem Substance ID:
329768469

Assay

97%

form

solid

reaction suitability

reaction type: Cross Couplings

mp

93-98 °C

SMILES string

CC(C)(C)[C@@H](CO1)N=C1C2=NC3=CC=CC=C3C=C2

InChI

1S/C16H18N2O/c1-16(2,3)14-10-19-15(18-14)13-9-8-11-6-4-5-7-12(11)17-13/h4-9,14H,10H2,1-3H3/t14-/m1/s1

InChI key

ZECIAWBAXVMXKI-CQSZACIVSA-N

Application

Ligand has been shown to influence high enantioselectivity in the asymmetric conjugate addition of boronic acids to enones under palladium catalysis.

Other Notes

Mechanism and Enantioselectivity in Palladium-Catalyzed Conjugate Addition of Arylboronic Acids to ß-Substituted Cyclic Enones: Insights from Computation and Experiment

related product

Product No.
Description
Pricing

901216

(S)-Ph-quinox, ≥95%

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

新产品

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