106213-67-6

Basic information

• Product Name: 5-(tert-butyl)-3-phenylisoxazole
• Synonyms: 5-(tert-butyl)-3-phenylisoxazole
• CAS NO: 106213-67-6
• Molecular Weight: 201.268
• Mol File: 106213-67-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-(tert-butyl)-3-phenylisoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(tert-butyl)-3-phenylisoxazole(106213-67-6)
• EPA Substance Registry System: 5-(tert-butyl)-3-phenylisoxazole(106213-67-6)

Safety Data

• Hazardous Substances Data: 106213-67-6(Hazardous Substances Data)

Upstream product

• 17475-11-5 1-phenyl-4,4-dimethylpent-2-yn-1-one 
• 98-88-4 benzoyl chloride 
• 917-92-0 3,3-Dimethylbut-1-yne 
• 870127-41-6 (Z)-4,4-dimethyl-1-phenyl-2-pentyn-1-one O-methyl oxime 
• 536-74-3 phenylacetylene 
• 292059-09-7 5-tert-butyl-5-hydroxy-3-phenyl-Δ²-isoxazoline 
• 13988-67-5 benzoylpivaloylmethane 
• 17474-12-3 4,4-dimethyl-1-phenyl-pent-2-yn-1-ol 
• 32398-67-7 4,4-dimethyl-1-phenyl-1-pentyn-3-one 
• 630-19-3 pivalaldehyde 

Relevant articles and documents

Complementary regioselective synthesis of 3,5-disubstituted isoxazoles from ynones

Two regioselective synthetic routes towards 3,5-disubstituted isoxazoles from ynones are reported. One route takes place via first converting the ynones to ynone O-methyl oximes, followed by a palladium-catalyzed intramolecular cyclization. The other invo

A versatile iron-catalyzed protocol for the one-pot synthesis of isoxazoles or isoxazolines from the same propargylic alcohols

The use N-sulfonyl-protected hydroxylamines as bi-nucleophiles in iron-catalyzed propargylic substitutions allows the selective one-pot synthesis of four classes of substituted isoxazoles or isoxazolines from the same propargylic alcohols (21 examples) by