209005-76-5

Basic information

• Product Name: exo-N-(p-hydroxyphenyl)-3,6-epoxy-4-cyclohexene-1,2-dicarboximide
• Synonyms: exo-N-(p-hydroxyphenyl)-3,6-epoxy-4-cyclohexene-1,2-dicarboximide
• CAS NO: 209005-76-5
• Molecular Weight: 257.246
• Mol File: 209005-76-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: exo-N-(p-hydroxyphenyl)-3,6-epoxy-4-cyclohexene-1,2-dicarboximide(CAS DataBase Reference)
• NIST Chemistry Reference: exo-N-(p-hydroxyphenyl)-3,6-epoxy-4-cyclohexene-1,2-dicarboximide(209005-76-5)
• EPA Substance Registry System: exo-N-(p-hydroxyphenyl)-3,6-epoxy-4-cyclohexene-1,2-dicarboximide(209005-76-5)

Safety Data

• Hazardous Substances Data: 209005-76-5(Hazardous Substances Data)

Upstream product

• 110-00-9 furan 
• 108-31-6 maleic anhydride 
• 123-30-8 4-amino-phenol 
• 6118-51-0 exo-3,6-epoxy-1,2,3,6-tetrahydrophthalic anhydride 

Downstream Products

• 300664-84-0 4-[2-(5-Chloro-2-methyl-thiophen-3-yl)-cyclopent-1-enyl]-5-methyl-thiophene-2-carboxylic acid 4-((1S,2R,6S,7R)-3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl)-phenyl ester 
• 499204-92-1 4-[3,3,4,4,5,5-Hexafluoro-2-(2-methyl-5-phenyl-thiophen-3-yl)-cyclopent-1-enyl]-5-methyl-thiophene-2-carboxylic acid 4-((1R,2S,6R,7S)-3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl)-phenyl ester 
• 391895-10-6 4-[2-(5-Chloro-2-methyl-thiophen-3-yl)-3,3,4,4,5,5-hexafluoro-cyclopent-1-enyl]-5-methyl-thiophene-2-carboxylic acid 4-((1R,2S,6R,7S)-3,5-dioxo-10-oxa-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl)-phenyl ester 

Relevant articles and documents

Novel photochromic homopolymers based on 1,2-Bis(3-thienyl)cyclopentenes

Incorporation of photochromic molecules into polymer matrices is necessary for materials applications such as optical information processing. Several novel homopolymers were prepared from l,2-bis(3-thienyl)cyclopentene derivatives using ring-opening metathesis polymerization techniques. Analysis by UV-vis absorption spectroscopy revealed that, in solution, they retained the appealing photochromic behavior exhibited by their respective monomers. The polymers were cast as thin films and spin-coated onto quartz substrates where the solid-state photochromic properties of the polymers were similar to those in solution.

Synthesis of Isoxazole-Linked Norcantharidin Analogues of Substituted Chromones

Eighteen novel norcantharidin derivatives, which were substituted by chromone ring, were synthesized in a single step by the [3 + 2] 1,3-dipolar cycloaddition reaction with three oximes in the presence of chloramine-T when compared with the conventional method.

Containing chromon structure-isoxazole Norcantharidin derivative and its preparation method and application

The invention discloses novel chromone structure containing isoxazole norcantharidin derivatives as well as a preparation method and an application thereof. The preparation method is characterized by introducing isoxazole rings to C5 and C6 in a norcantharidin structure by using a 1,3-dipolar cycloaddition method to react with chromone derivatives to import the chromone structures, thus synthesizing a series of totally six novel chromone structure containing isoxazole norcantharidin derivatives. The isoxazole norcantharidin derivatives are applied to synthesis of antitumor drugs and have broad application prospects.