| Identification | More | [Name]
5-Norbornene-2-carboxaldehyde | [CAS]
5453-80-5 | [Synonyms]
5-NORBORNENE-2-CARBALDEHYDE
5-NORBORNENE-2-CARBOXALDEHYDE
5-NORBORNENE-2-CARBOXALDEHYDE, ENDO AND EXO
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
TIMTEC-BB SBB005755
2-Formyl-5-norbornene
5-Formylbicyclo-2-heptene
5-Formylbicyclohept-2-ene
5-Norbornane-2-carboxaldehyde
5-norbornene-2-carboxaldehyde,mixtureofendoandexo
Bicyclo[2.2.1]hept-5-en-2-aldehyde
5-NORBORNENE-2-CARBOXALDEHYDE, 95%, MIXT URE OF ISOMERS
BICYCLO 2.2.1!HEPT-5-ENE-2-&
5-NORBORNENE-2-CARBOXALDEHYDE, ENDO + EXO, 95%
5-Norbornene-2-carboxaldehyde,endo+exo,95%
5-Norbornene-2-carboxaldehyde, mixture of endo and exo, 90-95%
5-Formyl-2-norbornene. | [EINECS(EC#)]
226-698-9 | [Molecular Formula]
C8H10O | [MDL Number]
MFCD00167568 | [Molecular Weight]
122.16 | [MOL File]
5453-80-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R10:Flammable.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S16:Keep away from sources of ignition-No smoking . | [RIDADR ]
UN 1989 3/PG 3
| [WGK Germany ]
3
| [TSCA ]
Yes | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29122990 |
| Hazard Information | Back Directory | [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. | [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. |
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