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2-(3,4-dichlorophenyl)-1,2-benzisothiazol-3(2H)-one, commonly known as DCBTO, is a chemical compound with the molecular formula C13H6Cl2NOS. It is a white to off-white crystalline solid that is widely used as a fungicide and algicide in various applications, including water treatment, agriculture, and industrial processes. DCBTO works by inhibiting the growth of fungi and algae by disrupting their cell membrane function. It is known for its broad-spectrum activity and effectiveness against a range of microorganisms. Due to its chemical structure, it is also referred to as a benzisothiazolone derivative. The compound is considered to be relatively stable and has a low potential for bioaccumulation, making it a preferred choice in certain applications where environmental impact is a concern. However, like any chemical, its use is regulated to ensure safety and efficacy.

4322-71-8

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4322-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4322-71-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4322-71:
(6*4)+(5*3)+(4*2)+(3*2)+(2*7)+(1*1)=68
68 % 10 = 8
So 4322-71-8 is a valid CAS Registry Number.

4322-71-8Downstream Products

4322-71-8Relevant academic research and scientific papers

Bioisosteric investigation of ebselen: Synthesis and in vitro characterization of 1,2-benzisothiazol-3(2H)-one derivatives as potent New Delhi metallo-β-lactamase inhibitors

Jin, Wen Bin,Xu, Chen,Cheung, Qipeng,Gao, Wei,Zeng, Ping,Liu, Jun,Chan, Edward W.C.,Leung, Yun-Chung,Chan, Tak Hang,Wong, Kwok-Yin,Chen, Sheng,Chan, Kin-Fai

, (2020/04/30)

Carbapenem-resistant Enterobacteriaceae (CRE) producing New Delhi metallo-β-lactamase (NDM-1) cause untreatable bacterial infections, posing a significant threat to human health. In the present study, by employing the concept of bioisosteric replacement of the selenium moiety of ebselen, we have designed, synthesized and characterized a small compound library of 2-substituted 1,2-benzisothiazol-3(2H)-one derivatives and related compounds for evaluating their cytotoxicity and synergistic activity in combination with meropenem against the E. coli Tg1 (NDM-1) strain. The most promising compound 3a demonstrated potent synergistic activity against a panel of clinically isolated NDM-1 positive CRE strains with FICI as low as 0.09. Moreover, its IC50 value and inhibition mechanism were also confirmed by using the enzyme inhibition assay and the ESI-MS analysis respectively. Importantly, compound 3a has acceptable toxicity and is not a PAINS. Because of its structural simplicity and potent synergistic activity in combination with meropenem, we propose that compound 3a may be a promising meropenem adjuvant and a new series of such compounds may worth further investigations.

1,2-BENZISOSELENAZOL-3(2H)-ONE AND 1,2-BENZISOTHIAZOL-3(2H)-ONE DERIVATIVES AS BETA-LACTAM ANTIBIOTIC ADJUVANTS

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Paragraph 0282-0285; 0290; 0291, (2019/10/04)

Provided herein are compositions and methods useful in the treatment of beta-lactam antibiotic resistant bacteria.

Treatment of rheumatism and arteriosclerosis with n-halogenophenyl-benzisothiazoles

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, (2008/06/13)

The invention relates to the new use of certain benzisothiazoles corresponding to the following general formula: STR1 wherein R1 represents chlorine, fluorine or bromine, and R2 represents hydrogen, chlorine, fluorine or bromine, in the treatment of phlogistic and/or arteriosclerotic processes.

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