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2-(2-(4-phenylpiperazin-1-yl)ethyl)benzo[d]isothiazol-3(2H)-one 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69211-49-0

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69211-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69211-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69211-49:
(7*6)+(6*9)+(5*2)+(4*1)+(3*1)+(2*4)+(1*9)=130
130 % 10 = 0
So 69211-49-0 is a valid CAS Registry Number.

69211-49-0Downstream Products

69211-49-0Relevant academic research and scientific papers

Benzyne-Induced Ring Opening Reactions of DABCO: Synthesis of 1,4-Disubstituted Piperazines and Piperidines

Seo, Jeongseob,Kim, Daegeun,Ko, Haye Min

, p. 2739 - 2743 (2020)

The 2-(4-phenylpiperazin-1-yl)ethan-1-amine scaffold is a structurally important motif that occurs frequently in medicinal and pharmaceutical chemistry. Despite the significance of this moiety, general strategies for its synthesis to date have required mu

2-Substituted benzisothiazol-3-ones

-

, (2008/06/13)

2-Substituted benzisothiazol-3-ones are provided having the structure STR1 wherein R is hydrogen, halogen, lower alkyl, lower alkoxy, or nitro; R1 is hydrogen, lower alkoxy or halogen, with the proviso that R1 can be lower alkoxy or halogen only when R is lower alkoxy or halogen, respectively; X is hydrogen, halogen, lower alkyl, lower alkoxy, or trifluoromethyl; Y is C or N, where Y is C, --------represents a single or double bond, and when Y is N, --------represents a single bond, p is 0 or 2, A is an alkylene group containing 2 to 5 carbons in the normal chain; and B is a single bond or an alkylene group containing from 1 to 3 carbons in the normal chain, and physiologically acceptable acid-addition salts thereof. These compounds have antiinflammatory activity, sedative and muscle relaxant activity. Pharmaceutical compositions containing such compounds and methods for using such compounds are also provided.

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