202191-12-6

Basic information

• Product Name: 2-(4,5-Dihydro-2-oxazolyl)quinoline 97%
• Synonyms: 2-(4,5-Dihydro-2-oxazolyl)quinoline 97%;2-(4,5-Dihydro-2-oxazolyl)quinoline
• CAS NO: 202191-12-6
• Molecular Formula: C12H10N2O
• Molecular Weight: 198
• Mol File: 202191-12-6.mol

Chemical Properties

• Melting Point: 109-110 °C
• Boiling Point: 380.2±15.0 °C(Predicted)
• Appearance: /
• Density: 1.26±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 3.27±0.61(Predicted)
• CAS DataBase Reference: 2-(4,5-Dihydro-2-oxazolyl)quinoline 97%(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4,5-Dihydro-2-oxazolyl)quinoline 97%(202191-12-6)
• EPA Substance Registry System: 2-(4,5-Dihydro-2-oxazolyl)quinoline 97%(202191-12-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/38
• Safety Statements: 26
• Hazardous Substances Data: 202191-12-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Applications:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure and properties make it a valuable building block in the development of new pharmaceutical compounds.
Used in Agrochemical Applications:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as an agrochemical intermediate for the development of new pesticides and other agrochemical products. Its high purity and unique structure make it a promising candidate for the creation of effective and environmentally friendly agrochemicals.
Used in Material Science Applications:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as a research compound in material science for the development of new materials with unique properties. Its high purity and versatile structure make it a valuable tool for researchers in the field of material science.
Used in Research and Development:
2-(4,5-Dihydro-2-oxazolyl)quinoline 97% is used as a research compound for further exploration of its potential applications in various fields. Its high purity and unique structure make it an ideal candidate for research and development efforts.

Upstream product

• 202191-13-7 N-(2-chloroethyl)quinoline-2-carboxamide 
• 5470-96-2 quinoline 2-carbaldehyde 
• 141-43-5 ethanolamine 
• 50342-01-3 quinolin-2-ylcarbonyl chloride 
• 93-10-7 quinoline-2-carboxylic acid 
• 100142-77-6 N-(2-hydroxyethyl)quinoline-2-carboxamide 

Relevant articles and documents

Concise Total Synthesis of (?)-Vermiculine through a Rhodium-Catalyzed C2-Symmetric Dimerization Strategy

A short and efficient synthesis of the C2-symmetric antibiotic (?)-vermiculine by utilizing an enantioselective catalytic one-step dimerization methodology as key-step to construct the core structure is reported. The late-stage modifications feature a double metathesis homologation followed by a double Wacker-type oxidation. These key-steps allowed the synthesis of vermiculine in only seven steps, starting from commercially available building blocks.

Synthesis of heterocyclic 1,3-oxazolines from aldehydes with trimethylphenylammonium tribromide

Various heterocyclic 1,3-oxazolines were prepared from aldehydes and aminoalcohols with trimethylphenylammonium tribromide at room temperature.

Pyridine-oxazoline and quinoline-oxazoline ligated cobalt complexes: Synthesis, characterization, and 1,3-butadiene polymerization behaviors

A series of cobalt complexes supported by pyridine-oxazoline (Pyox) and quinoline-oxazoline (Quox) were synthesized. Determined by single crystal X-ray crystallography, complexes 6a and 7c adopted distorted octahedron and trigonal bipyramid geometries, re

QUINOLINE-OXAZOLINE COMPOUNDS AND THEIR USE IN OXIDATION SYNTHESIS

A quinoline-oxazoline compound having the formula: where one of X1 and X2 is N and the other is C and one of R1, R2 and R3 is Z wherein Z is an oxazoline radical having the formula such that when X1 is N R2 is Z and R1 is absent, and when X2 is N either R1 or R3 is Z and R2 is absent. R1 and R3 through R12 are independently H or a pendant moiety which does not interfere with coordination of either N in the quinoline compound with a coordination center. These compounds can be complexed with a suitable coordination center such as catalytically active palladium and can be highly useful in catalytically oxidizing alkenes with high regioselectivity.

Catalyst-controlled Wacker-type oxidation of protected allylic amines

On the contrary: Utilizing the [Pd-(quinox)]-TBHP catalyst system, protected allylic amines were oxidized with high selectivity for the methyl ketone product. This is contrary to the results obtained by the substrate-controlled Tsuji-Wacker oxidation, which highlights the catalyst-controlled system presented here (see scheme). A variety of N-pro-tecting groups undergo selective oxidation with high ketone selectivity. TBHP = tert-butylhydroperoxide.