1314533-99-7 Usage
Uses
Used in Organic Synthesis:
(E)-ethyl 3-(2-ethoxypyriMidin-5-yl)acrylate is used as a building block in organic synthesis for the creation of pharmaceuticals and other biologically active molecules. Its unique structure allows for the development of new compounds with potential therapeutic properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (E)-ethyl 3-(2-ethoxypyriMidin-5-yl)acrylate serves as a valuable reagent. It is utilized to introduce pyrimidine and acrylate functional groups into organic molecules, which can lead to the discovery of novel drugs with improved efficacy and selectivity.
Used in Chemical Reactions:
(E)-ethyl 3-(2-ethoxypyriMidin-5-yl)acrylate is also employed as a reagent in chemical reactions, where its functional groups can be strategically incorporated into target molecules to enhance their chemical and biological properties.
Used in Agrochemical Industry:
(E)-ethyl 3-(2-ethoxypyriMidin-5-yl)acrylate may have potential applications in the agrochemical industry. It can be used as a precursor for the synthesis of herbicides and fungicides, contributing to the development of more effective and environmentally friendly products for agricultural use.
Check Digit Verification of cas no
The CAS Registry Mumber 1314533-99-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,5,3 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1314533-99:
(9*1)+(8*3)+(7*1)+(6*4)+(5*5)+(4*3)+(3*3)+(2*9)+(1*9)=137
137 % 10 = 7
So 1314533-99-7 is a valid CAS Registry Number.
1314533-99-7Relevant articles and documents
Feasible synthesis of the GPR40 antagonist by contructing 2-thiouracil ring VIA acid mediated cyclization
Zhao, Yongfeng,Liao, Jiayu
, p. 1145 - 1151 (2011)
GW1100 is an antagonist of GPR40 identified by high throughput screening recently. The feasible synthesis of GW1100 has been developed in mild conditions. The key step involves the cyclization of the 2-thiouracil heterocycle under acidic conditions at room temperature. The Japan Institute of Heterocyclic Chemistry.
The identification of a potent, water soluble inhibitor of lipoprotein-associated phospholipase A2
Boyd, Helen F.,Hammond, Beverley,Hickey, Deirdre M.B.,Ife, Robert J.,Leach, Colin A.,Lewis,Macphee, Colin H.,Milliner, Kevin J.,Pinto, Ivan L.,Smith, Stephen A.,Stansfield, Ian G.,Theobald, Colin J.,Whittaker, Caroline M.
, p. 701 - 704 (2007/10/03)
Modification of the pyrimidone 5-substituent in a series of 1-((amidolinked)-alkyl)-pyrimidones, lipophilic inhibitors of lipoprotein-associated phospholipase A2, has given inhibitors of nanomolar potency and improved physicochemical properties
