365242-41-7 Usage
Uses
Used in Pharmaceutical Industry:
2,3-DIMETHOXY-ACETOACETANILID is used as an intermediate in the synthesis of pharmaceutical compounds for its ability to react and form a variety of derivatives, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-DIMETHOXY-ACETOACETANILID is utilized as a reagent in organic synthesis, potentially aiding in the creation of new agrochemical products that can enhance crop protection and yield.
Caution:
It is crucial to handle and use 2,3-DIMETHOXY-ACETOACETANILID with care due to its potential hazards to human health and the environment. Proper safety measures should be implemented during its production, storage, and application to mitigate any risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 365242-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,2,4 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 365242-41:
(8*3)+(7*6)+(6*5)+(5*2)+(4*4)+(3*2)+(2*4)+(1*1)=137
137 % 10 = 7
So 365242-41-7 is a valid CAS Registry Number.
365242-41-7Relevant articles and documents
Synthesis of casimiroin and optimization of its quinone reductase 2 and aromatase inhibitory activities
Maiti, Arup,Reddy, P. V. Narasimha,Sturdy, Megan,Marler, Laura,Pegan, Scott D.,Mesecar, Andrew D.,Pezzuto, John M.,Cushman, Mark
experimental part, p. 1873 - 1884 (2009/12/31)
An efficient method has been developed to synthesize casimiroin (1), a component of the edible fruit of Casimiroa edulis, on a multigram scale in good overall yield. The route was versatile enough to provide an array of compound 1 analogues that were evaluated as QR2 and aromatase inhibitors. In addition, X-ray crystallography studies of QR2 in complex with compound 1 and one of its more potent analogues has provided insight into the mechanism of action of this new series of QR2 inhibitors. The initial biological investigations suggest that compound 1 and its analogues merit further investigation as potential chemopreventive or chemotherapeutic agents.
