2207-29-6

Usage

Uses

Used in Biochemical Research:
4-Chloro-7-nitro-2,1,3-benzothiadiazole is utilized as a fluorescent labeling agent for biomolecules, particularly proteins and nucleic acids, due to its ability to impart fluorescence to these molecules. This property is crucial for tracking and visualizing biomolecular interactions and dynamics within biological systems.
Used in the Synthesis of Fluorescent Dyes:
In the field of chemistry, 4-Chloro-7-nitro-2,1,3-benzothiadiazole is employed as a key component in the synthesis of fluorescent dyes. These dyes are essential for a variety of applications, including the development of new materials with specific optical properties and the creation of sensitive detection methods for various analytes.
Used in Sensor Development:
4-Chloro-7-nitro-2,1,3-benzothiadiazole is also used in the development of sensors, where its fluorescent characteristics can be harnessed to create responsive systems that detect changes in their environment, such as the presence of specific ions or molecules.
Used in Bioconjugation:
4-Chloro-7-nitro-2,1,3-benzothiadiazole is applied in bioconjugation processes, where it serves as a linker or a component of a conjugate that connects biologically active molecules with other entities, such as nanoparticles or other organic compounds, to create hybrid systems with novel functionalities.
Used in Molecular Imaging:
In molecular imaging, 4-Chloro-7-nitro-2,1,3-benzothiadiazole is used to enhance the visualization of biological structures and processes at the molecular level. Its fluorescent properties allow for the non-invasive monitoring of molecular events in living organisms.
Used in Spectroscopic Analysis:
4-Chloro-7-nitro-2,1,3-benzothiadiazole is employed in spectroscopic techniques, where its interaction with light can provide insights into the structure and dynamics of molecules, as well as the environments in which they are situated.

Upstream product

• 2207-28-5 4-Chlor-benz<2,1,3>thiadiazol 
• 21745-41-5 2,3-diaminochlorobenzene 
• 15777-35-2 4-chlorobenzo[c][1,2,5]selenadiazole 

Downstream Products

• 51323-01-4 4-Chlor-7-amino-benz<2.1.3>thiodiazol 

Relevant academic research and scientific papers

SCOTfluors: Small, Conjugatable, Orthogonal, and Tunable Fluorophores for In Vivo Imaging of Cell Metabolism

The transport and trafficking of metabolites are critical for the correct functioning of live cells. However, in situ metabolic imaging studies are hampered by the lack of fluorescent chemical structures that allow direct monitoring of small metabolites u

SMALL TUNABLE FLUOROPHORES FOR THE DETECTION AND IMAGING OF BIOMOLECULES

The invention relates to small, conjugatable, orthogonal and tunable fluorophores for imaging of small bioactive molecules. The invention further relates to processes for the preparation of the compounds, and uses of the compounds in therapeutic, diagnostic, surgery and analytical applications. The invention provides a compound of formula (I), a derivative or a salt thereof. Wherein X is selected from the group consisting of NH, O, S, SeR5R6, CR7R8; R1 is selected from the group consisting of amines, alcohols, thiols, thiophenols, selenols, selenophenols and aryl groups; R2 and R3 are independently H or a halogen; R4 is either H, nitro or cyano; R5 is either absent or methyl or oxygen; R6 is either absent or methyl or oxygen; and R7 and R8 are independently selected from the group consisting of linear or cyclic alkyl groups containing halogen, amino, cyano or carboxylic ester substituents, and alkyl aryl groups.

Agent and method for dyeing keratin fibers

The present invention relates to a fiber-dyeing agent (A) prepared by mixing two components (A1) and (A2), said agent being characterized in that component (A1) contains at least one compound of formula (I) 1wherein X denotes a halogen atom, a methoxy group or an ethoxy group; Y denotes an oxygen atom, a sulfur atom or a selenium atom; R1 and R2 are equal or different and independently of each other denote hydrogen, a halogen atom, a (C1-C4)-alkyl group, a halogen-substituted (C1-C4)-alkyl group, a (C1-C4)-alkoxy group, a nitro group, an acetamido group or an NRaRb group, wherein the Ra and Rb groups are equal or different and independently of each other denote hydrogen, a (C1-C4)-alkyl group, an optionally substituted aromatic carbon ring or a (C1-C4)-alkanecarbonyl group, or Ra and Rb together with the nitrogen atom form a heterocyclic (C3-C6) group, and component (A2) contains at least one compound from the group consisting of amines, aminonitrobenzenes and phenols; to a method for dyeing hair by use of said agent, and to a multicomponent kit.