119591-34-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The chemical structure describes the arrangement of atoms and the types of bonds between them in the compound.
Explanation
A preservative is a substance that is added to products to prevent spoilage, deterioration, or contamination.
Explanation
The compound is utilized in different industries for its antimicrobial properties, which help maintain the quality and longevity of products.
Explanation
The compound has the ability to kill or inhibit the growth of microorganisms, making it useful in controlling microbial contamination.
Explanation
The compound's antimicrobial and antifungal properties make it suitable for use in these industries to prevent the growth of harmful microorganisms.
Explanation
Due to its antimicrobial and antifungal properties, the compound may have potential uses in these industries for the development of new drugs or treatments.
Explanation
This is the IUPAC name of the compound, which provides a standardized way to identify and refer to the chemical.
Explanation
Synonyms are alternative names for a compound, which can be useful for searching or identifying the substance in different contexts.
Explanation
Physical properties such as color, state (solid, liquid, or gas), melting point, boiling point, and solubility are not mentioned in the material provided.
Chemical structure
Heterocyclic compound with a benzene ring fused to an isothiazole ring and a sulfur dioxide group.
Type of compound
Preservative
Industrial applications
Used in the production of various consumer products.
Antimicrobial properties
Acts as a biocide and fungicide.
Common uses
In the manufacturing of paints, adhesives, and metalworking fluids.
Potential applications
Pharmaceutical and agricultural industries.
Synonyms
Not provided in the material.
Physical properties
Not provided in the material.
Check Digit Verification of cas no
The CAS Registry Mumber 119591-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,5,9 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119591-34:
(8*1)+(7*1)+(6*9)+(5*5)+(4*9)+(3*1)+(2*3)+(1*4)=143
143 % 10 = 3
So 119591-34-3 is a valid CAS Registry Number.
119591-34-3Relevant academic research and scientific papers
Cai, Xinhong,Chen, Qiulu,Guan, Jing,Gong, Shunze,Fu, Hao,Xu, Defeng
, p. 1622 - 1624 (2017)
A convenient and concise synthesis of 2-methyl-5-nitrobenzene sulfonamide can be achieved by sulfochlorination and ammoniation with p-nitrotoluene as raw materials for an 81.2 % yield. 6-Aminosaccharin can be produced via oxidation and reduction in a 64.3
Preparation method of intermediate of iodosulfuron-methyl sodium
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Paragraph 0024-0029, (2019/09/16)
The invention discloses a preparation method of an intermediate of iodosulfuron-methyl sodium. The intermediate is obtained by performing a reaction on 6-aminosaccharin and potassium iodide in the presence of alkyl nitrite and acetic acid in one step, wherein a molar ratio of the potassium iodide to the 6-aminosaccharin is 1:1 to 1.2:1; a molar ratio of the alkyl nitrite to the 6-aminosaccharin is0.95:1 to 1:1; the alkyl nitrite is ethyl nitrite, isopropyl nitrite, n-butyl nitrite or isoamyl nitrite; and a molar ratio of the acetic acid to the 6-aminosaccharin is 1:1 to 1.2:1. According to the method provided by the invention, the alkyl nitrite is adopted for diazotization, the potassium iodide is added at the same time, so that decomposition and hydrolysis of a diazonium salt can be avoided, and the reaction yield is greatly improved; and the method does not require a large amount of water as a solvent and only adopts a small amount of water to wash an organic layer in the post-treatment, and therefore wastewater produced by adopting the method provided by the invention does not exceed 2 times the weight of the target product.
Design, synthesis and preliminary bioactivity studies of 1,2-dihydrobenzo[d]isothiazol-3-one-1,1-dioxide hydroxamic acid derivatives as novel histone deacetylase inhibitors
Han, Leiqiang,Wang, Lei,Hou, Xuben,Fu, Huansheng,Song, Weiguo,Tang, Weiping,Fang, Hao
, p. 1529 - 1538 (2014/03/21)
Histone deacetylase (HDAC) is a clinically validated target for antitumor therapy. In order to increase HDAC inhibition and efficiency, we developed a novel series of saccharin hydroxamic acids as potent HDAC inhibitors. Among them, compounds 11e, 11m, 11
