6-Nitro-2-benzothiazolinone (CAS 28620-12-4) is an organic compound characterized by its heterocyclic structure, which includes a benzothiazole ring with a nitro substituent. This compound typically appears as a yellow to orange crystalline solid and is known for its applications in various fields, including analytical chemistry and as a reagent in organic synthesis. It exhibits moderate solubility in organic solvents and limited solubility in water, which is common for many heterocyclic compounds. The presence of the nitro group contributes to its reactivity, making it useful in electrophilic substitution reactions. Additionally, 6-nitro-2-benzothiazolinone can act as a fluorescent probe, allowing for the detection of certain ions or molecules in solution. Safety considerations should be taken into account, as nitro compounds can be hazardous; thus, appropriate handling and disposal procedures are essential when working with this substance. Overall, its unique chemical properties make it a valuable compound in both research and industrial applications.

6-nitro-2-benzothiazolinone

28620-12-4: 2(3H)-Benzothiazolone, 6-nitro-, 6-Nitro-2(3H)-benzothiazolone, 6-nitro-1,3-benzothiazol-2(3H)-one

6-Nitro-2-benzothiazolinone is a nitroalkyl that is used in the synthesis of benzothiazolones. It is also used to produce 2-nitrobenzaldehyde, which can be used as a starting material for the production of other compounds. 6-Nitro-2-benzothiazolinone has been shown to promote the formation of callus tissue and shoots in cultured potato cells and has been suggested as a possible treatment for cancer. The mechanism of action may be due to its ability to activate cellular responses by mimicking an endogenous growth factor, or "pharmacophore".

CAS 28620-12-4: 6-nitro-2-benzothiazolinone

6-Nitro-2-benzothiazolinone

Ref: 3D-FN149821

2(3H)-Benzothiazolone, 6-nitro-

Ref: IN-DA002VVK

6-Nitro-2-benzothiazolinone

Ref: 54-OR322239

6-Nitrobenzo[d]thiazol-2(3H)-one

Ref: 10-F093366