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2,6-Bis(4,5-dihydrooxazol-2-yl)pyridine, 95%|2319863|165125-95-1

2,6-Bis(4,5-dihydrooxazol-2-yl)pyridine, 95%

Cat. No JK2319863_1_G
J&K Chemical

Product Information

Product Name
2,6-Bis(4,5-dihydrooxazol-2-yl)pyridine, 95%
Brand Name
J&K
Product Number
2319863
CAS
165125-95-1
Molecular Formula
C11H11N3O2
Molecular Weight
217.22
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
5242420
IUPAC Name
2-6-(4,5-dihydro-1,3-oxazol-2-yl)-2-pyridinyl-4,5-dihydro-1,3-oxazole
InChI Key
YOCRKHKJFCWTHG-UHFFFAOYSA-N
SMILES
C1COC(=N1)C2=NC(=CC=C2)C3=NCCO3

Properties

Melting Point
234-236

Safety Information

Storage Condition
Store at 2-8℃

References

Desymmetric sulfonylation of prochiral siladiols and related tandem sequences to multifunctional Si-chiral platform molecules
Publication Name: Science China Chemistry
Publication Date: 2025-07-22
DOI: 10.1007/s11426-025-2720-1

Construction of extremely low-symmetry double-stranded helicates based on terpyridine ligands with consecutive unsymmetrical modification
Publication Name: Science China Chemistry
Publication Date: 2025-01-17
DOI: 10.1007/s11426-024-2490-x

Enantioselective reductive conjugate alkenylation of α,β-enones with keto alkenyl acetates by nickel catalysis
Publication Name: Science China Chemistry
Publication Date: 2024-10-10
DOI: 10.1007/s11426-024-2181-5

Copper-catalyzed asymmetric dearomatizing amination of 2-naphthols: Csp2–N coupling via 1,3-reductive elimination
Publication Name: Science China Chemistry
Publication Date: 2024-07-02
DOI: 10.1007/s11426-024-2030-3

Dynamic steric confinement effect expands the frontier of Cu-catalyzed asymmetric propargylic aminations
Publication Name: Science China Chemistry
Publication Date: 2024-06-13
DOI: 10.1007/s11426-024-2127-9

2,6-Bis(4,5-dihydrooxazol-2-yl)pyridine, 95%

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