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| IUPAC Name: | 2-(2-bicyclo[2.2.1]hept-5-enyl)acetic acid |
| Description: | Carboxylic acid functionalized norbornene. Carboxylic acid can be used to modify amine containing compounds such as lysine residues on proteins/peptides via standard peptide coupling methods. Norbornene has been shown to react with 1,2,4,5-tetrazines in an inverse electron demand Diels-Alder cycloaddition reaction, which is a bioorthogonal click chemistry reaction demonstrated to be useful in biological imaging applications. |
| Molecular Weight: | 152.19 |
| Molecular Formula: | C9H12O2 |
| Canonical SMILES: | C1C2CC(C1C=C2)CC(=O)O |
| InChI: | InChI=1S/C9H12O2/c10-9(11)5-8-4-6-1-2-7(8)3-6/h1-2,6-8H,3-5H2,(H,10,11) |
| InChI Key: | HRVGJQMCNYJEHM-UHFFFAOYSA-N |
| Flash Point: | Not applicable |
| Density: | 1.124 g/mL at 25 ℃ |
| LogP: | 1.67330 |
| Refractive Index: | 1.495 |
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Ethyl 2-(allylamino)-4-(trifluoromethyl)thiazole-5-carboxylate
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