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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

Quality Level

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.

관련 제품

제품 번호
설명
가격

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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