42407-05-6

Basic information

• Product Name: 4,5-DIHYDRO-4,4-DIMETHYL-2-(4-NITROPHENYL)OXAZOLE
• Synonyms: 4,5-DIHYDRO-4,4-DIMETHYL-2-(4-NITROPHENYL)OXAZOLE
• CAS NO: 42407-05-6
• Molecular Formula: C₁₁H₁₂N₂O₃
• Molecular Weight: 220.22
• Mol File: 42407-05-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4,5-DIHYDRO-4,4-DIMETHYL-2-(4-NITROPHENYL)OXAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-DIHYDRO-4,4-DIMETHYL-2-(4-NITROPHENYL)OXAZOLE(42407-05-6)
• EPA Substance Registry System: 4,5-DIHYDRO-4,4-DIMETHYL-2-(4-NITROPHENYL)OXAZOLE(42407-05-6)

Safety Data

• Hazardous Substances Data: 42407-05-6(Hazardous Substances Data)

Upstream product

• 781-86-2 2,2-dimethyl-1-(4-nitrobenzoyl)aziridine 
• 1613-78-1 N-hydroxy-N-(1,1-dimethylethyl)-4-nitrobenzamide 
• 13793-40-3 2-Methyl-2-(4-nitrobenzamido)-propanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 124-68-5 2-Amino-2-methyl-1-propanol 
• 619-72-7 4-nitrobenzonitrile 
• 67-64-1 acetone 
• 4231-71-4 1H-1,2,3-benzotriazol-1-yl-4-nitrophenylmethanone 
• 62-23-7 4-nitro-benzoic acid 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 42449-40-1 8,8-dichloro-5-dichloromethylene-3,3-dimethyl-8a-(4-nitro-phenyl)-tetrahydro-oxazolo[3,2-c][1,3]oxazin-7-one 
• 42449-42-3 dichloro-[3-dichloroacetyl-4,4-dimethyl-2-(4-nitro-phenyl)-oxazolidin-2-yl]-acetic acid methyl ester 
• 1322669-58-8 C₂₀H₁₈ClN₃O 
• 69876-88-6 2-(4-aminophenyl)-4,4-dimethyl-2-oxazoline 

Relevant articles and documents

Silicon-rhodamine isothiocyanate for fluorescent labelling

An efficient synthesis for silicon-rhodamines was developed, enabling the preparation and evaluation of silicon-rhodamine isothiocyanate (SITC) as a novel tool for facile fluorescent labeling. Ease of use in conjugation to amino groups, high stability and excellent photophysical properties are demonstrated. SITC-actin was found to be neutral to F-actin polymerization induction and well suited for high resolution fluorescence microscopy.

Facile Syntheses of Oxazolines and Thiazolines with N-Acylbenzotriazoles under Microwave Irradiation

Microwave reactions of 2-amino-2-methyl-1-propanol (2) or 2-aminoethanethiol hydrochloride (4) with readily available N-acylbenzotriazoles 1a-j in the presence of SOCl2 produced 2-substituted 2-oxazolines 3a-j in 84-98% yields and 2-substituted

Natural Kaolinitic clay catalyzed conversion of nitriles to 2-oxazolines

Natural Kaolinitic clay has been found effective as catalyst in the conversion of aromatic and aliphatic nilriles with 1,2-aminoalcohol to 2-oxazolines (56-96%, yield).