(E)-Cyclooct-4-enol,

Code: 764396-50mg D2-231

Not available outside of the UK & Ireland.

Application

Hydroxyl modified cyclooctene derivative. Cyclooctenes are useful in strain-promoted copper-free click chemistry cycloaddition reactions with 1,2,4,5-tetrazines. ...


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Your Price
$868.30 50MG

Not available outside of the UK & Ireland.

Application

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.

(E)-Cyclooct-4-enol may be used in the multi-step synthesis of trans-cyclooctene geranyl diphosphate, a novel strained-ring containing protein farnesyltransferase (PFTase) substrate that can be used in site-specific modification technologies.

Packaging

10, 50 mg in glass bottle

formliquid
InChI keyUCPDHOTYYDHPEN-CMLYIYFCSA-N
InChI1S/C8H14O/c9-8-6-4-2-1-3-5-7-8/h1-2,8-9H,3-7H2/b2-1+/t8-/m0/s1
reaction suitabilityreaction type: click chemistry
SMILES stringO[C@H]1CC/C=C/CCC1
storage temp.−20°C
Cas Number85081-69-2
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