2,5-dioxopyrrolidin-1-yl 3-(pyridin-2-yldisulfanyl)butanoate - CAS 107348-47-0

2,5-dioxopyrrolidin-1-yl 3-(pyridin-2-yldisulfanyl)butanoate - CAS 107348-47-0 Catalog number: BADC-00486

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

Category
ADCs Linker
Product Name
2,5-dioxopyrrolidin-1-yl 3-(pyridin-2-yldisulfanyl)butanoate
CAS
107348-47-0
Catalog Number
BADC-00486
Molecular Formula
C13H14N2O4S2
Molecular Weight
326.39
2,5-dioxopyrrolidin-1-yl 3-(pyridin-2-yldisulfanyl)butanoate

Ordering Information

Catalog Number Size Price Quantity
BADC-00486 -- $--
Inquiry
Synonyms
(2,5-dioxopyrrolidin-1-yl) 3-(pyridin-2-yldisulfanyl)butanoate
Canonical SMILES
CC(CC(=O)ON1C(=O)CCC1=O)SSC2=CC=CC=N2
InChI
InChI=1S/C13H14N2O4S2/c1-9(20-21-10-4-2-3-7-14-10)8-13(18)19-15-11(16)5-6-12(15)17/h2-4,7,9H,5-6,8H2,1H3
InChIKey
VQZYZXLBKBUOHE-UHFFFAOYSA-N
Density
1.43g/cm3
Flash Point
237.3°C
Index Of Refraction
1.634
LogP
0.54770
PSA
131.35000
Vapor Pressure
5.81E-09mmHg at 25°C
Appearance
Soild powder
Purity
≥98%
Shipping
Room temperature
Boiling Point
468.8°C at 760mmHg

2,5-Dioxopyrrolidin-1-yl 3-(pyridin-2-yldisulfanyl)butanoate is a versatile compound with significant potential in biochemical research and industrial applications. Here are some key applications of this compound:

Organic Synthesis: The compound can be used as a reagent in organic synthesis, particularly for the formation of disulfide bonds. It facilitates the introduction of sulfur atoms into molecular frameworks, making it invaluable for constructing sulfur-containing heterocycles. This is crucial for developing novel pharmaceuticals and materials with sulfur functionalities.

Bioconjugation: In the realm of biochemistry, 2,5-dioxopyrrolidin-1-yl 3-(pyridin-2-yldisulfanyl)butanoate is employed in bioconjugation reactions where it acts as a linker between biomolecules. It is particularly effective for attaching a wide range of tags or labels to proteins and peptides. This capability is essential for applications in protein tracking, imaging, and therapeutic delivery.

Redox Research: This compound can serve as a redox agent in biochemical experiments aimed at studying oxidative stress and redox regulatory mechanisms. Its disulfide bonds can participate in redox cycling, thus allowing the investigation of cellular responses to oxidative conditions. Understanding these mechanisms helps in developing antioxidant therapies and redox-based diagnostic tools.

Drug Delivery Systems: Researchers can utilize this compound in designing sophisticated drug delivery systems. Its disulfide linkage allows for the creation of redox-responsive carriers that release payloads in environments with specific redox conditions. This targeted release approach enhances the efficacy and reduces the side effects of therapeutics, making it a promising strategy in precision medicine.

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

Why Choose BOC Sciences?

Customer Support

Providing excellent 24/7 customer service and support

Project Management

Offering 100% high-quality services at all stages

Quality Assurance

Ensuring the quality and reliability of products or services

Global Delivery

Ensuring timely delivery of products worldwide

Questions & Comments
Verification code
Send Inquiry
Verification code
Inquiry Basket