43221-63-2

Basic information

• Product Name: Oxazole, 4,5-dihydro-2-(3-methylphenyl)-
• CAS NO: 43221-63-2
• Molecular Formula: C10H11NO
• Molecular Weight: 161.203
• Mol File: 43221-63-2.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Oxazole, 4,5-dihydro-2-(3-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazole, 4,5-dihydro-2-(3-methylphenyl)-(43221-63-2)
• EPA Substance Registry System: Oxazole, 4,5-dihydro-2-(3-methylphenyl)-(43221-63-2)

Safety Data

• Hazardous Substances Data: 43221-63-2(Hazardous Substances Data)

Upstream product

• 1711-06-4 3-Methylbenzoyl chloride 
• 99-04-7 m-Toluic acid 
• 141-43-5 ethanolamine 
• 620-22-4 3-Methylbenzonitrile 
• 778623-19-1 3-methyl-benzoic acid-(2-hydroxy-ethylamide) 
• 134-62-3 N,N-Diethyl-3-methylbenzamide 
• 500131-50-0 N,N-diethyl-α,α-difluoro-(meta-methylbenzyl)amine 
• 620-23-5 m-tolyl aldehyde 

Downstream Products

• 1021602-68-5 C₂₀H₂₀N₂O₂ 
• 1119513-04-0 bis-(2-[m-tolyl]-2-oxazoline-κ1N) zinc(II) bromide 
• 1119512-97-8 bis-(2-[m-tolyl]-2-oxazoline-κ1N) zinc(II) chloride 
• 1314961-45-9 7-methyl-3-phenyl-1H-2-benzopyran-1-one 

Relevant articles and documents

Polynuclear copper(ii) pyrazolate complexes: Temperature-dependent protonolysis reactions, crystal structures and high catalytic activity toward the condensation of nitriles with 2-aminoalcohol

Reaction of Cu(OAc)2·H2O and 1H-pyrazole-3,5-dicarboxylic acid dimethyl ester (Hdcmpz) in MeOH at room temperature afforded one tetranuclear Cu(ii)/pyrazolate complex [{Cu 2(μ-OAc)2}2(μ-dcmpz)2/

Oxazolinyl-Assisted Ru(II)-Catalyzed C-H Allylation with Allyl Alcohols and Synthesis of 4-Methyleneisochroman-1-ones

We report herein a ruthenium-catalyzed, oxazoline-directed strategy for C-H allylation of aryl oxazolines using allylic alcohols as the coupling partner. The present transformation unravels the unusual reactivity of allylic alcohols in the synthesis of 4-

Highly efficient synthesis of β-nitrate ester carboxamides through the ring-opening of 2-oxazolines

A novel method for the synthesis of β-nitrate ester carboxamides using non-corrosive tert-butyl nitrite (TBN) as the nitro source and easily available oxygen as the oxidant has been developed. Variously substituted 2-oxazolines were efficiently ring-opened to deliver the corresponding products in excellent yields. Notably, this reaction provides fast access to pharmaceuticals such as nicorandil.