55099-10-0

Basic information

• Product Name: 4-(3,5-DIOXO-4-AZA-TRICYCLO[5.2.1.0(2,6)]DEC-8-EN-4-YL)-BENZOIC ACID
• Synonyms: 4-(3,5-DIOXO-4-AZA-TRICYCLO[5.2.1.0(2,6)]DEC-8-EN-4-YL)-BENZOIC ACID;4-(1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-4,7-methanoisoindol-2-yl)benzoic acid
• CAS NO: 55099-10-0
• Molecular Formula: C16H13NO4
• Molecular Weight: 283.28
• Mol File: 55099-10-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(3,5-DIOXO-4-AZA-TRICYCLO[5.2.1.0(2,6)]DEC-8-EN-4-YL)-BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3,5-DIOXO-4-AZA-TRICYCLO[5.2.1.0(2,6)]DEC-8-EN-4-YL)-BENZOIC ACID(55099-10-0)
• EPA Substance Registry System: 4-(3,5-DIOXO-4-AZA-TRICYCLO[5.2.1.0(2,6)]DEC-8-EN-4-YL)-BENZOIC ACID(55099-10-0)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 55099-10-0(Hazardous Substances Data)

Upstream product

• 150-13-0 4-amino-benzoic acid 
• 129-64-6 3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride 
• 826-62-0 5-norbornene-2,3-dicarboxylic anhydride 

Downstream Products

• 61800-57-5 2-exo-hydroxy-5-oxo-4-oxatricyclo[4.2.1.0^3,7]nonane-9-carboxylic acid 

Relevant articles and documents

Pillararene-containing polymers with tunable fluorescence properties based on host–guest interactions

Linear polymers containing pillar[5]arenes as the pendant groups were designed and synthesized via a ring-opening metathesis polymerization. Such polymers could form supramolecular brush polymers and exhibited tunable fluorescence properties based on the host–guest interactions.

Azobenzene-containing side-chain ionic metathesis polymers: Facile synthesis, self-assembly and photoresponsive behavior

A series of well-defined azobenzene-functionalized ionomers were produced via ring-opening metathesis polymerization of norbornene-dicarboximide tethered to an ionic group further connected with an azobenzene unit in ionic liquid. The corresponding azobenzene-containing non-ionic polymers were also synthesized by the similar method. All the polymerizations were confirmed to be the characteristic of living based on the linear relationship between molecular weight and feed ratio. As expected, the distinct photoresponsive properties from azobenzene units in ionomers were observed under alternating irradiation of UV and visible light, which cannot be achieved by traditional azobenzene-containing non-ionic polymers. The ability and efficiency of trans?cis photoisomerization was depressed to some extent due to the presence of ionic groups nearby azobenzene units. Moreover, the sizes and morphologies of these ionomers can be modulated through changing the number of the methylene spacer to generate regular and uniform spherical nanostructures, ultimately leading to the unique photoisomerization behaviors. All these interesting results will not only provide a facile and efficient method for constructing photosensitive ionic metathesis polymers, but also expand the optical properties and application prospect of azobenzene-containing polymers.

Novel oligomers useful for making cured fibre reinforced composites

The invention provides a compound of the general formula I STR1 in which R1 is hydrogen or methyl and R2 is C1 -C12 alkyl, preferably methyl or ethyl.