4-Nitro-2,1,3-benzothiadiazole is an organic compound characterized by its heterocyclic structure, which includes a benzene ring fused to a thiadiazole moiety. This compound features a nitro group (-NO2) at the 4-position of the benzothiadiazole ring, contributing to its chemical reactivity and potential applications. It is typically a yellow to orange crystalline solid, exhibiting moderate solubility in organic solvents. The presence of the nitro group enhances its electron-withdrawing properties, making it useful in various chemical reactions, including nucleophilic substitutions and as a precursor for synthesizing other compounds. 4-Nitro-2,1,3-benzothiadiazole is often utilized in the fields of materials science, organic electronics, and as a dye or pigment due to its chromophoric properties. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as nitro-substituted compounds can be hazardous.

4-Nitro-2,1,3-benzothiadiazole

6583-06-8: 2,1,3-Benzothiadiazole, 4-nitro-, 4-Nitropiazthiole, NSC 404747, 4-Nitro-2,1,3-benzothiadiazole

4-Nitro-2,1,3-benzothiadiazole is a nitro group acceptor that has been shown to be able to form stable complexes with metal ions through coordination chemistry. It can act as an electron-donor when attached to the ribosomal subunit and can be used as a technique in quantum theory. 4-Nitro-2,1,3-benzothiadiazole has been shown to be a promising candidate for the study of damaged DNA and is currently being researched for its use in proteomic studies. The quantum theory of 4-Nitro-2,1,3-benzothiadiazole is based on gaseous measurement techniques and functional theory.

CAS 6583-06-8: 4-Nitro-2,1,3-benzothiadiazole

4-Nitro-2,1,3-benzothiadiazole

Ref: 3B-N0786

4-Nitro-2,1,3-benzothiadiazole

Ref: 3D-GAA58306

4-Nitro-benzo[1,2,5]thiadiazole

Ref: 54-OR97403

4-Nitro-2,1,3-benzothiadiazole

Ref: 10-F045796

4-Nitrobenzo[c][1,2,5]thiadiazole

Ref: IN-DA003LUL