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Merck
모든 사진(1)

주요 문서

764523

Sigma-Aldrich

(E)-Cyclooct-4-enyl 2,5-dioxo-1-pyrrolidinyl carbonate

동의어(들):

(E)-4-Cycloocten-1-yl 2,5-dioxo-1-pyrrolidinyl ester carbonic acid, trans-4-Cycloocten-1-yl 2,5-dioxo-1-pyrrolidinyl carbonate, TCO-N-hydroxysuccinimidyl carbonate, TCO-NHS, TCO-carbonate

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About This Item

실험식(Hill 표기법):
C13H17NO5
CAS Number:
Molecular Weight:
267.28
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.22

양식

solid

반응 적합성

reaction type: click chemistry
reagent type: linker

mp

90-105 °C

작용기

NHS ester

저장 온도

−20°C

SMILES string

O=C(ON1C(CCC1=O)=O)O[C@@H]2CC/C=C/CCC2

InChI

1S/C13H17NO5/c15-11-8-9-12(16)14(11)19-13(17)18-10-6-4-2-1-3-5-7-10/h1-2,10H,3-9H2/b2-1+/t10-/m1/s1

InChI key

OUGQJOKGFAIFAQ-TXXBHVLJSA-N

애플리케이션

(E)-Cyclooct-4-enyl 2,5-dioxo-1-pyrrolidinyl carbonate may be used in the synthesis of vancomycin-TCO that can bind to the cell wall of gram-positive bacteria, which can subsequently react with tetrazine (Tz) decorated magneto-fluorescent nanoparticles orthogonally. This bioorthogonal labeling method is useful for the detection of gram-positive bacteria.
Succinimidyl carbonate/NHS functionalized cyclooctene derivative for incorporation of the cyclooctene moiety into amine containing compounds or biomolecules. 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.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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