Other grades of this product :
| rel-(1R,4E,pR)-Cyclooct-4-enol Basic information |
| Product Name: | rel-(1R,4E,pR)-Cyclooct-4-enol | | Synonyms: | (4E)-4-Cycloocten-1-ol;(E)-Cyclooct-4-enol;rel-(1R,4E,pR)-Cyclooct-4-enol;TCO-OH;trans-Cyclooctenol;(4E)-TCO-OH;TCO-OH,TCO-hydroxyl;4-Cycloocten-1-ol, (4E)- | | CAS: | 85081-69-2 | | MF: | C8H14O | | MW: | 126.2 | | EINECS: | | Product Categories: | | Mol File: | 85081-69-2.mol |
| rel-(1R,4E,pR)-Cyclooct-4-enol Chemical Properties |
| Boiling point | 202.2±29.0 °C(Predicted) | | density | 0.954±0.06 g/cm3(Predicted) | | storage temp. | -20°C | | pka | 15.13±0.20(Predicted) |
| Hazard Codes | Xi | | Risk Statements | 41-52 | | Safety Statements | 26-39 | | WGK Germany | 3 |
| rel-(1R,4E,pR)-Cyclooct-4-enol Usage And Synthesis |
| Description | TCO-OH is a TCO intermediate allowed for further derivatizion | | Uses | Hydroxyl modified cyclooctene derivative. Cyclooctenes are useful in strain-promoted copper-free click chemistry cycloaddition reactions with 1,2,4,5-tetrazines. This cyclooctene will react with tetrazine functionalized compounds or biomolecules without the need for a catalyst to result in a stable covalent linkage. The 4+2 inverse electron demand Diels-Alder cycloaddition between trans-cyclooctene and tetrazines is the fastest biologically compatible ligation technology reported and has had many applications in biological labeling and imaging. |
| rel-(1R,4E,pR)-Cyclooct-4-enol Preparation Products And Raw materials |
|
日本语
한국어
Français
Deutsch
España
Türkiye