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(S)-4-tert-Butyl-2-(2-pyridyl)oxazoline, 98%|1682830|117408-98-7

(S)-4-tert-Butyl-2-(2-pyridyl)oxazoline, 98%

Cat. No JK1682830_250_MG
J&K Chemical

Product Information

Product Name
(S)-4-tert-Butyl-2-(2-pyridyl)oxazoline, 98%
Brand Name
J&K
Product Number
1682830
CAS
117408-98-7
Molecular Formula
C12H16N2O
Molecular Weight
204.27
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
S)-4-(tert-Butyl)-2-(2-pyridyl)-4,5-dihydrooxazole
PubChem CID
14337774
IUPAC Name
(4S)-4-tert-butyl-2-pyridin-2-yl-4,5-dihydro-1,3-oxazole
InChI Key
JDOAIDZRVWJBEG-SNVBAGLBSA-N
SMILES
CC(C)(C)C@H1COC(=N1)C2=CC=CC=N2

Properties

Melting Point
70.0 - 74.0
Optical Activity
-75.0 to -79.0 ° (C = 1, CH2Cl2)

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
Precautionary Statement
P280
P321
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317

References Data Source From Pubchem

Fluorination of Alkenes or Alkynes
Publication Name: Science of Synthesis
Publication Date: 2025

Ni-catalysed assembly of axially chiral alkenes from alkynyl tetracoordinate borons via 1,3-metallate shift
Publication Name: Nature Chemistry
Publication Date: 2024-01
DOI: 10.1038/s41557-023-01396-7

8-Quinolinyl Oxazoline: Ligand Exploration in Enantioselective Ni-Catalyzed Reductive Carbamoyl-Alkylation of Alkene to Access the Chiral Oxindoles
Publication Name: Synlett
Publication Date: 2022-07-08
DOI: 10.1055/a-1863-8957

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

Nickel-Catalyzed Regiodivergent Reductive Hydroarylation of Styrenes
Publication Name: Synlett
Publication Date: 2021-06-23
DOI: 10.1055/a-1523-3228

(S)-4-tert-Butyl-2-(2-pyridyl)oxazoline, 98%

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