24033-98-5 Usage
Nitrosoaniline derivative
This compound belongs to the class of nitrosoaniline derivatives, which are organic compounds containing a nitro group (-NO2) and an amine group (-NH2) in their structure.
Dye intermediate
2-[(4-methoxy-2-nitrophenyl)sulfanyl]aniline is commonly used as a dye intermediate in the production of organic pigments and reactive dyes, which are coloring agents for various industries.
Dark red solid
The physical appearance of this compound is a dark red solid, indicating its color and state of matter.
Solubility
Sparingly soluble in water, more soluble in organic solvents
2-[(4-methoxy-2-nitrophenyl)sulfanyl]aniline has limited solubility in water, meaning it does not dissolve easily in water. However, it dissolves more readily in organic solvents, such as alcohols and ethers.
Potential anti-tumor agent
This compound has shown potential in medical research as an anti-tumor agent due to its ability to induce apoptosis (cell death) in cancer cells, making it a possible candidate for cancer treatment.
Mutagenic compound
2-[(4-methoxy-2-nitrophenyl)sulfanyl]aniline is known to be mutagenic, meaning it can cause changes in the genetic material (DNA) of cells, which may lead to mutations and other adverse effects.
Safety precautions
Due to its mutagenic properties, caution must be taken when handling and disposing of 2-[(4-methoxy-2-nitrophenyl)sulfanyl]aniline to ensure safe and proper management, minimizing the risk of exposure and potential harm.
Check Digit Verification of cas no
The CAS Registry Mumber 24033-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,3 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24033-98:
(7*2)+(6*4)+(5*0)+(4*3)+(3*3)+(2*9)+(1*8)=85
85 % 10 = 5
So 24033-98-5 is a valid CAS Registry Number.
24033-98-5Relevant articles and documents
N-Acylaminophenothiazines: Neuroprotective agents displaying multifunctional activities for a potential treatment of Alzheimer's disease
González-Mu?oz, Gema C.,Arce, Mariana P.,López, Beatriz,Pérez, Concepción,Romero, Alejandro,Barrio, Laura Del,Martín-De-Saavedra, María Dolores,Egea, Javier,León, Rafael,Villarroya, Mercedes,López, Manuela G.,García, Antonio G.,Conde, Santiago,Rodríguez-Franco, María Isabel
body text, p. 2224 - 2235 (2011/06/22)
We have previously reported the multifunctional profile of N-(3-chloro-10H-phenothiazin-10-yl)-3-(dimethylamino)propanamide (1) as an effective neuroprotectant and selective butyrylcholinesterase inhibitor. In this paper, we have developed a series of N-acylaminophenothiazines obtained from our compound library or newly synthesised. At micro- and sub-micromolar concentrations, these compounds selectively inhibited butyrylcholinesterase (BuChE), protected neurons against damage caused by both exogenous and mitochondrial free radicals, showed low toxicity, and could penetrate into the CNS. In addition, N-(3-chloro-10H-phenothiazin-10-yl)-2-(pyrrolidin-1-yl) acetamide (11) modulated the cytosolic calcium concentration and protected human neuroblastoma cells against several toxics, such as calcium overload induced by an l-type Ca2+-channel agonist, tau-hyperphosphorylation induced by okadaic acid and Aβ peptide.
