おすすめの製品
フォーム
solid
反応適合性
reaction type: click chemistry
reagent type: linker
官能基
amine
保管温度
−20°C
SMILES記法
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
アプリケーション
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.
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
790451-VAR:
790451-50MG:
790451-BULK:
790451-10MG:
最新バージョンのいずれかを選択してください：
この製品を見ている人はこちらもチェック
![(1R,8S,9s)-ビシクロ[6.1.0]ノナ-4-イン-9-イルメタノール for Copper-free Click Chemistry](/deepweb/assets/sigmaaldrich/product/structures/171/632/0556139a-2db5-4678-a6ec-a26a693fd574/640/0556139a-2db5-4678-a6ec-a26a693fd574.png)
![9-Oxabicyclo[6.1.0]non-4-ene 95%](/deepweb/assets/sigmaaldrich/product/structures/328/338/c44d0a8d-81ab-4a17-81bb-aebb26a006e7/640/c44d0a8d-81ab-4a17-81bb-aebb26a006e7.png)
Mark R Karver et al.
Bioconjugate chemistry, 22(11), 2263-2270 (2011-09-29)
1,2,4,5-Tetrazines have been established as effective dienes for inverse electron demand [4 + 2] Diels-Alder cycloaddition reactions with strained alkenes for over 50 years. Recently, this reaction pair combination has been applied to bioorthogonal labeling and cell detection applications; however
Neal K Devaraj et al.
Bioconjugate chemistry, 19(12), 2297-2299 (2008-12-05)
Bioorthogonal tetrazine cycloadditions have been applied to live cell labeling. Tetrazines react irreversibly with the strained dienophile norbornene forming dihydropyrazine products and dinitrogen. The reaction is high yielding, selective, and fast in aqueous media. Her2/neu receptors on live human breast
Melissa L Blackman et al.
Journal of the American Chemical Society, 130(41), 13518-13519 (2008-09-19)
Described is a bioorthogonal reaction that proceeds with unusually fast reaction rates without need for catalysis: the cycloaddition of s-tetrazine and trans-cyclooctene derivatives. The reactions tolerate a broad range of functionality and proceed in high yield in organic solvents, water
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
製品に関するお問い合わせはこちら（テクニカルサービス）