90628-79-8

Basic information

• Product Name: (3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate
• CAS NO: 90628-79-8
• Molecular Formula: C₁₃H₁₀FN₃O₆S
• Molecular Weight: 355.2984
• Mol File: 90628-79-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 527.3°C at 760 mmHg
• Flash Point: 272.7°C
• Density: 1.619g/cm³
• Vapor Pressure: 3.31E-11mmHg at 25°C
• Refractive Index: 1.651
• CAS DataBase Reference: (3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate(90628-79-8)
• EPA Substance Registry System: (3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate(90628-79-8)

Safety Data

• Hazardous Substances Data: 90628-79-8(Hazardous Substances Data)

Usage

Description

(3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate is a chemical compound with the molecular formula C13H10FN3O5S. It is a versatile intermediate in organic syntheses, characterized by the presence of a nitro group, a ureido group, and a fluoro-phenyl-sulfonate group. (3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate is recognized for its ability to crosslink proteins and other biomolecules, making it a valuable tool in biochemical and immunological research. Furthermore, it holds potential in drug discovery and development due to its capacity to modify the structure and activity of biomolecules. However, it is crucial to handle this compound with care due to its potential hazardous properties.

Uses

Used in Research Applications:
(3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate is used as a labeling reagent for the synthesis of peptides and proteins, serving as an essential tool in research settings. Its unique functional groups facilitate the attachment of labels to biomolecules, aiding in the study of their structure, function, and interactions.
Used in Biochemical and Immunological Studies:
In the field of biochemistry and immunology, (3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate is utilized for its crosslinking capabilities. It helps in stabilizing protein structures and can be instrumental in the development of immunoassays and other diagnostic tools.
Used in Drug Discovery and Development:
(3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate is employed as a key intermediate in the development of new drugs. Its ability to modify the structure and activity of biomolecules can lead to the discovery of novel therapeutic agents with improved efficacy and selectivity.
Used in Organic Syntheses:
(3-nitro-4-ureido-phenyl) 4-fluorobenzenesulfonate is also used in various organic syntheses across different chemical industries. Its functional groups make it a valuable building block for the creation of complex organic molecules and pharmaceutical intermediates.