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2-[(4S)-4-(1,1-Dimethylethyl)-4,5-dihydro-2-oxazolyl]-5-(trifluoromethyl)pyridine, 97%, ee: 98%|1528294|1416819-91-4

2-[(4S)-4-(1,1-Dimethylethyl)-4,5-dihydro-2-oxazolyl]-5-(trifluoromethyl)pyridine, 97%, ee: 98%

Cat. No JK1528294_500_MG
J&K Chemical

Product Information

Product Name
2-(4S)-4-(1,1-Dimethylethyl)-4,5-dihydro-2-oxazolyl-5-(trifluoromethyl)pyridine, 97%, ee: 98%
Brand Name
J&K
Product Number
1528294
CAS
1416819-91-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
71712916
IUPAC Name
(4S)-4-tert-butyl-2-5-(trifluoromethyl)-2-pyridinyl-4,5-dihydro-1,3-oxazole
InChI Key
AATATIAROAAKIN-SNVBAGLBSA-N
SMILES
CC(C)(C)C@H1COC(=N1)C2=NC=C(C=C2)C(F)(F)F

Safety Information

Storage Condition
Freezer -20℃

References

Recent Advances in Transition-Metal-Catalyzed Asymmetric Functionalization of Enamides
Publication Name: Synthesis
Publication Date: 2022-08-18
DOI: 10.1055/a-1892-5473

Acyclic Quaternary Carbon Stereocenters through Transition-Metal-Catalyzed Enantioselective Functionalization of Unsaturated Hydrocarbons
Publication Name: Synthesis
Publication Date: 2022-03-01
DOI: 10.1055/s-0040-1719899

Transition-Metal-Catalyzed Enantioselective Synthesis of Indoles from 2-Alkynylanilines
Publication Name: Synthesis
Publication Date: 2022-02-22
DOI: 10.1055/a-1729-9572

Nickel-Catalyzed Enantioselective Two-Component Reductive Arylalkenylation of Alkenes
Publication Name: Science of Synthesis
Publication Date: 2022

Indolylcyclopentenes through an Enantioselective Aminopalladation–Heck Reaction
Publication Name: Synfacts
Publication Date: 2021-05-18
DOI: 10.1055/s-0040-1720662

2-[(4S)-4-(1,1-Dimethylethyl)-4,5-dihydro-2-oxazolyl]-5-(trifluoromethyl)pyridine, 97%, ee: 98%

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