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4-Isopropyl-zimtsaeure-N,N-diethylamid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42174-82-3

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42174-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42174-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,7 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42174-82:
(7*4)+(6*2)+(5*1)+(4*7)+(3*4)+(2*8)+(1*2)=103
103 % 10 = 3
So 42174-82-3 is a valid CAS Registry Number.

42174-82-3Downstream Products

42174-82-3Relevant academic research and scientific papers

Copper-catalyzed synthesis of α,β-unsaturated acylamides via direct amidation from cinnamic acids and N-substituted formamides

Yan, Hong,Yang, Hailong,Lu, Linhua,Liu, Defu,Rong, Guangwei,Mao, Jincheng

supporting information, p. 7258 - 7263 (2013/08/23)

A highly effective synthesis of α,β-unsaturated acylamides is reported for the first time via copper-catalyzed direct amidation between readily available cinnamic acids and N-substituted formamides. The protocol was easily accessible and practical.

Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells

Germain, Andrew R.,Carmody, Leigh C.,Nag, Partha P.,Morgan, Barbara,Verplank, Lynn,Fernandez, Cristina,Donckele, Etienne,Feng, Yuxiong,Perez, Jose R.,Dandapani, Sivaraman,Palmer, Michelle,Lander, Eric S.,Gupta, Piyush B.,Schreiber, Stuart L.,Munoz, Benito

supporting information, p. 1834 - 1838 (2013/04/10)

A high-throughput screen (HTS) was conducted against stably propagated cancer stem cell (CSC)-enriched populations using a library of 300,718 compounds from the National Institutes of Health (NIH) Molecular Libraries Small Molecule Repository (MLSMR). A cinnamide analog displayed greater than 20-fold selective inhibition of the breast CSC-like cell line (HMLE-sh-Ecad) over the isogenic control cell line (HMLE-sh-eGFP). Herein, we report structure-activity relationships of this class of cinnamides for selective lethality towards CSC-enriched populations.

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