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| | 5-Norbornene-2-carboxaldehyde Basic information |
| Product Name: | 5-Norbornene-2-carboxaldehyde | | Synonyms: | 2-Formyl-5-norbornene;5-Formylbicyclo-2-heptene;5-Formylbicyclohept-2-ene;AKOS BC-0598;BICYCLO[2.2.1]-5-HEPTEN-2-YL METHANAL;BICYCLO[2.2.1]HEPT-5-ENE-2-CARBALDEHYDE;BICYCLO[2.2.1]HEPT-5-ENE-2-CARBOXALDEHYDE;5-NORBORNENE-2-CARBOXALDEHYDE, 95%, MIXT URE OF ISOMERS | | CAS: | 5453-80-5 | | MF: | C8H10O | | MW: | 122.16 | | EINECS: | 226-698-9 | | Product Categories: | Norbornene Derivatives | | Mol File: | 5453-80-5.mol |  |
| | 5-Norbornene-2-carboxaldehyde Chemical Properties |
| Hazard Codes | Xi | | Risk Statements | 10-36/37/38 | | Safety Statements | 23-37/39-26-16 | | RIDADR | UN 1989 3/PG 3 | | WGK Germany | 3 | | TSCA | Yes | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29122990 |
| | 5-Norbornene-2-carboxaldehyde Usage And Synthesis |
| Chemical Properties | clear colorless to yellow liquid | | Uses | 5-Norbornene-2-carboxaldehyde was used in transition metal-catalyzed synthesis of norbornene-derived homopolymers having pendent t-Boc-protected quinizarin moieties for patterned fluorescence images. It acts as Diels-Alder adduct of acrolein and cyclopentadiene. It can be used as protected form of acrolein, from which the double bond may be liberated by cycloreversion, e.g. in a useful synthesis of 2-vinylimidazole. |
| | 5-Norbornene-2-carboxaldehyde Preparation Products And Raw materials |
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