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(4-isopentyloxy-phenyl)-acetonitrile is an organic compound with the chemical formula C12H15NO. It is a derivative of acetonitrile, featuring a 4-isopentyloxy-phenyl group attached to the acetonitrile molecule. (4-isopentyloxy-phenyl)-acetonitrile is characterized by its aromatic ring structure, with an isopentyl group (a five-carbon alkyl chain) attached to the para position of the phenyl ring, and a nitrile group (C≡N) at the end of the acetonitrile chain. It is a colorless to pale yellow liquid with a mild, aromatic odor. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and other specialty chemicals. Its unique structure allows for a range of applications, making it a valuable component in the chemical industry.

50690-56-7

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50690-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50690-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,9 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50690-56:
(7*5)+(6*0)+(5*6)+(4*9)+(3*0)+(2*5)+(1*6)=117
117 % 10 = 7
So 50690-56-7 is a valid CAS Registry Number.

50690-56-7Upstream product

50690-56-7Relevant academic research and scientific papers

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Freudenreich, Charles,Samama, Jean-Pierre,Biellmann, Jean-Francois

, p. 3344 - 3353 (2007/10/02)

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.

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