92789-63-4

Basic information

• Product Name: C₁₅H₁₁NO₅
• Synonyms: C₁₅H₁₁NO₅
• CAS NO: 92789-63-4
• Molecular Weight: 285.256
• Mol File: 92789-63-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₅H₁₁NO₅(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₁₁NO₅(92789-63-4)
• EPA Substance Registry System: C₁₅H₁₁NO₅(92789-63-4)

Safety Data

• Hazardous Substances Data: 92789-63-4(Hazardous Substances Data)

Upstream product

• 873-67-6 benzonitrile oxide 
• 5426-09-5 7-oxanorborn-5-ene-2,3-dicarboxylic anhydride 
• 6118-51-0 exo-3,6-epoxy-1,2,3,6-tetrahydrophthalic anhydride 

Downstream Products

• 91937-72-3 3-phenyl-(3aξ,7aξ)-3a,4,5,6,7,7a-hexahydro-4,7-epioxido-benzo[d]isoxazole-5c,6c-dicarboxylic acid dimethyl ester 
• 93945-90-5 3-phenyl-(3aξ,7aξ)-3a,4,5,6,7,7a-hexahydro-4r,7c-epioxido-benzo[d]isoxazole-5c,6c-dicarboxylic acid 

Relevant articles and documents

PREPARATION AND PHOTOCHEMISTRY OF FUROISOXAZOLINES. AN EXTRAORDINARILY UNAMBIGUOUS PHOTO-INDUCED REARRANGEMENT

Preparation and photolysis of furoisoxazoline derivatives is described.The respective compounds IVa, II and VI were obtained by a 1,3-dipolar cycloadition of benzenenitrile oxide to 5,6-dimethoxycarbonyl-7-oxabicyclo-2-heptene, 2,5-dihydrofuran and furan; IVb was synthesized from benzoylnitrile oxide.The biradical primarily formed by photolysis was stabilized with respect to the arrangement of the heteroatom and the isoxazoline chromophore.The new 1,3-oxazine derivatives III and V were obtained in high yields as single products.The quantum yield of photoreaction of II, IVa and XXVII was found to be 0.04, 0.26 and 0.07 respectively.Were the stabilization of the radical by conjugation with the lone electron pair of oxygen impossible, oxazoline VII should be formed.Photolysis of the benzoyl derivative IVb had an anomalous course and yielded the β-aminochalcone Xb.