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N-Acetyl-5-chlor-anilin-disulfonsaeure-(2.4)-dichlorid, also known as N-Acetyl-5-chloroaniline disulfonic acid dichloride, is a chemical compound with the molecular formula C8H7Cl2NO5S2. It is a derivative of aniline, featuring a chloro substituent at the 5-position and an acetyl group at the nitrogen atom. The disulfonic acid group provides two sulfonic acid functionalities, which contribute to its water solubility and potential for further chemical reactions. N-Acetyl-5-chlor-anilin-disulfonsaeure-(2.4)-dichlorid is typically synthesized for use in the production of dyes and pigments, where its specific functional groups can be utilized to create a range of colors and properties. It is important to handle N-Acetyl-5-chlor-anilin-disulfonsaeure-(2.4)-dichlorid with care due to its potential reactivity and the presence of multiple chlorine atoms, which can contribute to environmental concerns if not managed properly.

1029-80-7

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1029-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1029-80-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1029-80:
(6*1)+(5*0)+(4*2)+(3*9)+(2*8)+(1*0)=57
57 % 10 = 7
So 1029-80-7 is a valid CAS Registry Number.

1029-80-7Relevant academic research and scientific papers

Synthesis, characterization, and investigation of the antioxidant activity of some 1,2,4-benzothiadiazine-1,1-dioxides bearing sulfonylthioureas moieties

Harrouche, Kamel,Lahouel, Asma,Belghobsi, Mebrouk,Pirotte, Bernard,Khelili, Smail

, p. 824 - 832 (2019/11/28)

A series of 1,2,4-benzothiadiazine-1,1-dioxides bearing a sulfonylthiourea moiety were synthesized, characterized, and screened for their antioxidant activity, using six antioxidant analytical assays comparatively to reference compounds, ascorbic acid and quercetin. The results indicated that several compounds demonstrated strong antioxidant activity in DPPH, ABTS, H2O2, and lipid peroxidation assays where some of them were either as active as or more active than reference compounds. However, all compounds were largely less active than references compounds in the reducing power assay. The results indicated that the thiourea moiety probably played a crucial role in the antioxidant activity of the target compounds, as a thiolate ion. The most favorable R1 groups were the hydrogen atom and methyl group, followed by phenyl and benzyl groups, whereas the most favorable R2 group was iPr, followed by the phenyl and methyl groups. The combination of benzothiadiazine ring with sulfonylthiourea moieties led to valuable new antioxidants, which could be used in the treatment or the prevention of certain diseases or in the field of cosmetics, which needs further investigations in the future.

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