50690-53-4 Usage
Description
(4-Isopropoxyphenyl)acetonitrile, with the CAS number 941217-48-8, is a white to beige solid compound characterized by its molecular formula C11H13NO. It is a nitrile, which means it contains a carbon triple-bonded to a nitrogen atom, and is also an acetonitrile derivative, featuring an acetonitrile functional group. The presence of phenyl and isopropoxy groups in its structure makes it a versatile compound for use in organic reactions, particularly for the synthesis of complex molecules with medicinal or agricultural applications. However, it is important to note that (4-Isopropoxyphenyl)acetonitrile has moderate toxicity, and therefore, it should be handled with caution.
Uses
Used in Pharmaceutical Industry:
(4-Isopropoxyphenyl)acetonitrile is used as an intermediate in the synthesis of pharmaceuticals for its ability to participate in organic reactions that lead to the creation of complex molecules with medicinal purposes.
Used in Agrochemical Industry:
(4-IsoPROPOXYPHENYL)ACETONITRILE is used as an intermediate in the synthesis of agrochemicals for its capacity to engage in organic reactions that result in the formation of complex molecules with agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 50690-53-4 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 50690-53:
(7*5)+(6*0)+(5*6)+(4*9)+(3*0)+(2*5)+(1*3)=114
114 % 10 = 4
So 50690-53-4 is a valid CAS Registry Number.
50690-53-4Relevant articles and documents
Synthesis of lamellarin alkaloids using orthoester-masked α-keto acids
Shirley, Harry J.,Koyioni, Maria,Muncan, Filip,Donohoe, Timothy J.
, p. 4334 - 4338 (2019/04/17)
Pyruvic acid and other α-keto acids are frequently encountered as intermediates in metabolic pathways, yet their application in total synthesis has met with limited success. In this work, we present a bioinspired strategy that utilizes highly functionaliz
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.