169776-89-0

Basic information

• Product Name: 2-[(4R)-4,5-dihydro-4-phenyl-1,3-oxazolin-2-yl]benzenamine
• Synonyms: 2-[(4R)-4,5-dihydro-4-phenyl-1,3-oxazolin-2-yl]benzenamine
• CAS NO: 169776-89-0
• Molecular Weight: 238.289
• Mol File: 169776-89-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-[(4R)-4,5-dihydro-4-phenyl-1,3-oxazolin-2-yl]benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4R)-4,5-dihydro-4-phenyl-1,3-oxazolin-2-yl]benzenamine(169776-89-0)
• EPA Substance Registry System: 2-[(4R)-4,5-dihydro-4-phenyl-1,3-oxazolin-2-yl]benzenamine(169776-89-0)

Safety Data

• Hazardous Substances Data: 169776-89-0(Hazardous Substances Data)

Upstream product

• 875-74-1 (R)-phenylglycine 
• 118-48-9 isatoic anhydride 
• 56613-80-0 D-2-phenylglycinol 
• 1885-29-6 anthranilic acid nitrile 

Downstream Products

• 169776-90-3 (4R)-{2-[2-(tolylsulfonyl)amino]phenyl}-4-phenyloxazoline 

Relevant articles and documents

A Novel Synthesis of 1,2,3-Benzotriazinones from 2-(o -Aminophenyl)oxazolines

1,2,3-Benzotriazinones were synthesized in excellent yields by the reaction of 2-(o-aminophenyl)oxazolines and isoamyl nitrite in methanol. The crystal structure of the acetyl derivative of one of the 1,2,3-benzotriazinones provided additional support for

Significant Enhancement of Circularly Polarized Luminescence Dissymmetry Factors in Quinoline Oligoamide Foldamers with Absolute Helicity

When S- or R- oxazolylaniline enantiomers were attached to achiral quinoline oligoamide foldamers (QOFs), a single diastereomerically pure P- or M-handed foldamer was observed and exhibits negative or positive circularly polarized luminescence with the em

Nicotinamide compound containing chiral oxazoline and application of same as agricultural bactericide

The invention relates to a novel nicotinamide compound containing chiral oxazoline and application of the compound as an agricultural bactericide. The compound has a chemical structural formula as shown in a formula (I) which is described in the specifica

The novel reaction of ketones with o-oxazoline-substituted anilines

A variety of ketones react with o-oxazoline-substituted anilines in the presence of catalytic amount of p-toluenesulfonic acid in dry n-butanol to form 4-amino-substituted quinolines or 4-quinolones in fair to good yields.