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5-(benzyloxy)-2-(prop-1-en-2-yl)pyridine is a complex organic chemical compound characterized by a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. In this specific compound, the pyridine ring is substituted at the 5-position with a benzyloxy group, which is a benzyl group (a phenylmethyl group) attached to an oxygen atom. Additionally, at the 2-position, there is a prop-1-en-2-yl group, which is a propene chain with a double bond between the first and second carbon atoms. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain active ingredients. Its structure and properties make it a valuable component in the development of new compounds with specific therapeutic or pesticidal effects.

1196074-40-4

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1196074-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1196074-40-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,0,7 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1196074-40:
(9*1)+(8*1)+(7*9)+(6*6)+(5*0)+(4*7)+(3*4)+(2*4)+(1*0)=164
164 % 10 = 4
So 1196074-40-4 is a valid CAS Registry Number.

1196074-40-4Relevant academic research and scientific papers

Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives

Westaway, Susan M.,Preston, Alex G. S.,Barker, Michael D.,Brown, Fiona,Brown, Jack A.,Campbell, Matthew,Chung, Chun-Wa,Drewes, Gerard,Eagle, Robert,Garton, Neil,Gordon, Laurie,Haslam, Carl,Hayhow, Thomas G.,Humphreys, Philip G.,Joberty, Gerard,Katso, Roy,Kruidenier, Laurens,Leveridge, Melanie,Pemberton, Michelle,Rioja, Inma,Seal, Gail A.,Shipley, Tracy,Singh, Onkar,Suckling, Colin J.,Taylor, Joanna,Thomas, Pamela,Wilson, David M.,Lee, Kevin,Prinjha, Rab K.

, p. 1370 - 1387 (2016/03/05)

Following the discovery of cell penetrant pyridine-4-carboxylate inhibitors of the KDM4 (JMJD2) and KDM5 (JARID1) families of histone lysine demethylases (e.g., 1), further optimization led to the identification of non-carboxylate inhibitors derived from pyrido[3,4-d]pyrimidin-4(3H)-one. A number of exemplars such as compound 41 possess interesting activity profiles in KDM4C and KDM5C biochemical and target-specific, cellular mechanistic assays.

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