产品说明
应用
Amine functionalized trans-cyclooctene derivative for incorporation of the cyclooctene moiety into carboxyl containing compounds or biomolecules via standard coupling techniques (DCC; EDC etc...). Trans-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.
包装
10, 50 mg in clear glass bottle
基本信息
经验(实验)分子式 | C12H22N2O2 · HCl |
分子量 | 262.78 |
PubChem化学物质编号 | 329768216 |
NACRES | NA.22 |
产品性质
reaction suitability | reaction type: click chemistry |
质量水平 | 100 |
储存温度 | −20℃ |
SMILES string | O=C(NCCCN)OC1CCC/C=C/CC1.[H]Cl |
InChI | 1S/C12H22N2O2.ClH/c13-9-6-10-14-12(15)16-11-7-4-2-1-3-5-8-11;/h1-2,11H,3-10,13H2,(H,14,15);1H/b2-1+; |
InChI key | GIYQQURLGCGUKK-TYYBGVCCSA-N |
安全信息
象形图 | |
警示用语: | Warning |
危险声明 | H302 |
危险分类 | Acute Tox. 4 Oral |
储存分类代码 | 11 - Combustible Solids |
WGK | WGK 3 |
闪点(F) | Not applicable |
闪点(C) | Not applicable |
Sigma-Aldrich