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2-hydroxybenzyl (4'-aminosulfonylphenyl) amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13159-86-9

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13159-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13159-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13159-86:
(7*1)+(6*3)+(5*1)+(4*5)+(3*9)+(2*8)+(1*6)=99
99 % 10 = 9
So 13159-86-9 is a valid CAS Registry Number.

13159-86-9Downstream Products

13159-86-9Relevant academic research and scientific papers

Design, synthesis, evaluation and 3D-QSAR analysis of benzosulfonamide benzenesulfonates as potent and selective inhibitors of MMP-2

Qiu, Han-Yue,Wang, Zhong-Chang,Wang, Peng-Fei,Yan, Xiao-Qiang,Wang, Xiao-Ming,Yang, Yong-Hua,Zhu, Hai-Liang

, p. 39214 - 39225 (2014)

A novel series of MMPIs was designed, synthesized and purified using a scaffold modification strategy. The new compounds were also evaluated for biological activity against A549, MCF-7, HepG2 and Hela as potential inhibitors of MMP-2. The most potent inhi

Synthesis of 4-sulfamoylphenyl-benzylamine derivatives with inhibitory activity against human carbonic anhydrase isoforms I, II, IX and XII

Durgun, Mustafa,Turkmen, Hasan,Ceruso, Mariangela,Supuran, Claudiu T.

, p. 982 - 988 (2016/02/19)

Imine derivatives were obtained by condensation of sulfanilamide with substituted aromatic aldehydes. The Schiff bases were thereafter reduced with sodium borohydride, leading to the corresponding amines, derivatives of 4-sulfamoylphenyl-benzylamine. These sulfonamides were investigated as inhibitors of the human carbonic anhydrase (hCA, EC 4.2.1.1) isoforms hCA I and II (cytosolic isozymes), as well as hCA IX and XII (transmembrane, tumor-associated enzymes). We noted that the compounds incorporating secondary amine moieties showed a better inhibitory activity against all CA isozymes compared to the corresponding Schiff bases. Low nanomolar CA II, IX and XII inhibitors were detected, whereas the activity against hCA I was less potent. The secondary amines incorporating sulfonamide or similar zinc-binding groups, poorly investigated chemotypes for designing metalloenzyme inhibitors, may offer interesting opportunities in the field due to the facile preparation and possibility to explore a vast chemical space.

SODIUM BOROHYDRIDE REDUCTION OF AROMATIC SULFONYL AZIDES IN THE PRESENCE OR ABSENCE OF TELLURIUM

Obafemi, Craig. A.,Onigbinde, Adebayo O.

, p. 75 - 81 (2007/10/02)

Some aromatic sulfonyl azides have been reduced, in various solvents, with sodium borohydride, in the presence or absence of Te element to the corresponding sulfonamides.Other functionals groups like the imino group may also be reduced.

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