1580501-97-8

(2E)-TCO-PNB ester Chemical Structure
1580501-97-8

Chemical Structure

(2E)-TCO-PNB ester

  • CAS No.: 1580501-97-8
  • Formula:C15H17NO5
  • Molecular Weight:291.30

IUPAC Name: (E)-cyclooct-2-en-1-yl (4-nitrophenyl) carbonate

InChIKey: XNTGBHHUEQUWSQ-GQCTYLIASA-N

SMILES: O=C(OC1=CC=C([N+]([O-])=O)C=C1)OC2/C=C/CCCCC2

Biological Activity: (2E)-TCO-PNB ester is an active reaction substrate with the properties of trans-cyclooctene derivatives. The core chemical property of (2E)-TCO-PNB ester is its ability to undergo efficient inverse electron-demand Diels-Alder (IEDDA) cycloaddition with tetrazine groups. (2E)-TCO-PNB ester can be used in ligation reactions to verify the integrity of tetrazine groups, and also serves as a key synthetic raw material for the preparation of the prodrug TCO-DOX. (2E)-TCO-PNB ester is applied in research related to drug synthesis and bioorthogonal chemistry[1][2].

Cat. No. Product Name Purity Description Pricing
HY-134599
(2E)-TCO-PNB ester 99.46% (2E)-TCO-PNB ester is an active reaction substrate with the properties of trans-cyclooctene derivatives. The core chemical property of (2E)-TCO-PNB ester is its ability to undergo efficient inverse electron-demand Diels-Alder (IEDDA) cycloaddition with tetrazine groups. (2E)-TCO-PNB ester can be used in ligation reactions to verify the integrity of tetrazine groups, and also serves as a key synthetic raw material for the preparation of the prodrug TCO-DOX. (2E)-TCO-PNB ester is applied in research related to drug synthesis and bioorthogonal chemistry.
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This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References