1108603-35-5

Basic information

• Product Name: 2-[(4R)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]- Pyridine
• Synonyms: 2-[(4R)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]- Pyridine;2-[(4R)-4,5-Dihydro-4-(phenylmethyl)-2- oxazolyl]pyridine,98%e.e.
• CAS NO: 1108603-35-5
• Molecular Formula: C15H14N2O
• Molecular Weight: 238.28446
• Mol File: 1108603-35-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 402.0±18.0 °C(Predicted)
• Appearance: /
• Density: 1.16±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 3.73±0.70(Predicted)
• CAS DataBase Reference: 2-[(4R)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]- Pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4R)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]- Pyridine(1108603-35-5)
• EPA Substance Registry System: 2-[(4R)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]- Pyridine(1108603-35-5)

Safety Data

• Hazardous Substances Data: 1108603-35-5(Hazardous Substances Data)

Usage

General Description

"2-[(4R)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]- Pyridine" is a chemical compound that consists of a pyridine ring with a 2-oxazolyl group attached at the 4-position and a phenylmethyl group attached to the 4R position. It is a chiral compound, with the (4R) stereochemistry indicating that the substituents are arranged in a specific configuration. 2-[(4R)-4,5-dihydro-4-(phenylMethyl)-2-oxazolyl]- Pyridine may have potential biological activity and may be of interest for research in medicinal chemistry or pharmacology. However, further studies would be needed to fully understand its properties and potential applications.

Upstream product

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Relevant articles and documents

Palladium-Catalyzed C-2 C-H Heteroarylation of Chiral Oxazolines: Diverse Synthesis of Chiral Oxazoline Ligands

A direct, efficient, and practical protocol to install a chiral oxazoline unit onto aryl/heteroaryl rings via palladium-catalyzed C-H functionalization of 2-positions of oxazolines with a variety of halides using dppe as the ligand has been developed. Var

Parallel screening of asymmetric bidentate ligands in zinc catalyzed transfer hydrogenation

Development in the field of asymmetric catalysis is driven by the importance of stereochemically pure compounds in the field of pharmaceutical industry, agrochemicals and flavors. The unpredictable results given by new catalysts make the design of effecti

Rapid, in situ synthesis of bidentate ligands: Chromatography-free generation of catalyst libraries

The parallel synthesis of chiral bidentate ligands and their subsequent use in situ for a catalytic process is described. The ligands thus prepared gave comparable results to those obtained when the ligands were synthesized and purified by conventional means. This includes oxazolines and other compounds of similar complexity, meaning that for the first time these valuable compounds have been brought into the field of combinatorial catalysis.