4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate - CAS 874302-76-8

4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate - CAS 874302-76-8 Catalog number: BADC-00458

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Category
ADCs Linker
Product Name
4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate
CAS
874302-76-8
Catalog Number
BADC-00458
Molecular Formula
C14H12N2O5S2
Molecular Weight
352.39
4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate

Ordering Information

Catalog Number Size Price Quantity
BADC-00458 -- $--
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Synonyms
(4-nitrophenyl) 2-(pyridin-2-yldisulfanyl)ethyl carbonate;
Canonical SMILES
C1=CC=NC(=C1)SSCCOC(=O)OC2=CC=C(C=C2)[N+](=O)[O-]
InChI
InChI=1S/C14H12N2O5S2/c17-14(21-12-6-4-11(5-7-12)16(18)19)20-9-10-22-23-13-3-1-2-8-15-13/h1-8H,9-10H2
InChIKey
JHDROZPIXZYTMZ-UHFFFAOYSA-N
Appearance
Soild powder
Purity
≥98%
Shipping
Room temperature, or blue ice upon request.

4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate is a chemical reagent with specific applications in chemical synthesis and biochemical studies. Here are some key applications of this compound:

Protein Labeling and Modification: 4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate is used in protein chemistry for the selective labeling and modification of sulfhydryl groups. It reacts with cysteine residues in proteins, introducing a disulfide bond that can facilitate further conjugation steps. This is valuable in the creation of protein conjugates and the study of protein interactions.

Enzyme Activity Probes: This compound is employed as an enzyme activity probe in biochemical assays. By incorporating it into substrates, researchers can monitor enzyme-catalyzed reactions through the release of the nitrophenol moiety, which can be quantified spectrophotometrically. This allows for the assessment of enzymatic activity in various biological samples.

Drug Delivery Systems: 4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate can be used in the design of drug delivery systems where a controlled release of payloads is required. The disulfide bond in the compound can be cleaved in reductive environments, such as inside cells, leading to the release of therapeutic agents. This property is leveraged to develop redox-sensitive drug carriers for targeted delivery.

Bioconjugation Reactions: In the field of bioconjugation, this reagent facilitates the coupling of biomolecules like nucleic acids, peptides, and antibodies to other functional entities. By enabling specific and stable conjugation through disulfide linkages, it serves in the preparation of complex bioconjugates used in diagnostics, imaging, and therapeutics.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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