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Methanesulfonamide, N-[2-(1-methylethoxy)-4-nitrophenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

169211-11-4

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169211-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169211-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,1 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 169211-11:
(8*1)+(7*6)+(6*9)+(5*2)+(4*1)+(3*1)+(2*1)+(1*1)=124
124 % 10 = 4
So 169211-11-4 is a valid CAS Registry Number.

169211-11-4Downstream Products

169211-11-4Relevant articles and documents

New nimesulide derivatives with amide/sulfonamide moieties: Selective COX-2 inhibition and antitumor effects

Güng?r, Tu?ba,Ozleyen, Adem,Y?lmaz, Yakup Berkay,Siyah, Pinar,Ay, Mehmet,Durda??, Serdar,Tumer, Tugba Boyunegmez

, (2021)

Seventeen new amide/sulfonamide containing nimesulide derivatives were synthesized and characterized by several spectroscopic techniques and primarily investigated for their inhibitory potential on COX enzymes and other pro-inflammatory factors. Experimen

Synthesis of carbon-11 labeled sulfonanilide analogues as new potential PET agents for imaging of aromatase in breast cancer

Wang, Min,Lacy, Gabrielle,Gao, Mingzhang,Miller, Kathy D.,Sledge, George W.,Zheng, Qi-Huang

, p. 332 - 336 (2007/10/03)

Aromatase is a particularly good target in the treatment of estrogen receptor positive breast cancer. Novel carbon-11 labeled sulfonanilide analogues, N-[11C]methyl-N-(2-alkyloxy-4-nitrophenyl)-methanesulfonamide s ([11C]3a-f, alkyl

SULFONANILIDE ANALOGS AS SELECTIVE AROMATASE MODULATORS

-

Page/Page column title page; 19; 1/15, (2010/11/28)

Compounds and methods suppressing aromatase activity expression in cancer cells. Provided are compounds are those of formula I: wherein R1 may be alkyl, cycloakyl, haloalkyl, aryl, substituted aryl, haloaryl, alkoxy, alkylaryl, and arylalkyl; R2 is H, alk

Novel sulfonanilide analogues suppress aromatase expression and activity in breast cancer cells independent of COX-2 inhibition

Su, Bin,Diaz-Cruz, Edgar S.,Landini, Serena,Brueggemeier, Robert W.

, p. 1413 - 1419 (2007/10/03)

Aromatase is a particularly attractive target in the treatment of estrogen receptor positive breast cancer. Aromatase levels in breast cancer cells are enhanced by prostaglandins and reduced by COX inhibitors. The synthesis and biological evaluation of a

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