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3-(o-tolylamino)benzo[d]isothiazole 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108666-47-3

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108666-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108666-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,6 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108666-47:
(8*1)+(7*0)+(6*8)+(5*6)+(4*6)+(3*6)+(2*4)+(1*7)=143
143 % 10 = 3
So 108666-47-3 is a valid CAS Registry Number.

108666-47-3Downstream Products

108666-47-3Relevant academic research and scientific papers

Synthesis, characterization and antimicrobial evaluation of new 3-(Alkyl/Arylamino)benzo[d]isothiazole 1,1-derivatives

Kamble, Dhanraj P.,Shankarwar, Anil G.,Mane, Yogesh D.,Tigote, Radhakrishna M.,Sarnikar, Yuvaraj P.,Madje, Balaji R.

, p. 797 - 804 (2021/09/08)

The saccharine nucleus has long been recognized as a significant component in medicine. A series of pseudo-saccharine amines derivatives (7a-j) were synthesized and examined for their antibacterial activity. After testing all compounds, 7b, 7f, 7g, 7i and 7j were found most effective against Escherichia coli, Streptococcus aureus and Bacillus subtilis strains. The MIC of the compound was found from 4.6 to 16.1 μM. Further, compound 7f and 7i exhibited excellent activity against E.coli and Bacillus subtilis with MIC value 4.6 and 4.7 μM respectively. The compound 7b and 7i was found active against all the three bacteria. The zone inhibition was observed at 10 μM against Escherichia coli, Staphylococcus aureus and Bacillus subtilis at 0.9, 1.8, 3.9 respectively for 7b and 1.0, 1.8 and 2.0 cm respectively for 7i.

Synthesis and Spectroscopic Properties of Some New Substituted Saccharin Anils

Salman, Salman R.,Subber, Amjad K.,Hussein, F. A.,Shubber, S. K.

, p. 391 - 393 (2007/10/02)

Fourteen new substituted saccharin anils have been synthesized by the reaction of pseudosaccharin chloride with various substituted anilines.The IR, proton NMR, and carbon-13 NMR spectral properties are presented and discussed.

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