220151-12-2 Usage
Uses
Used in Pharmaceutical Production:
Ethyl 4-(2-bromoethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylate serves as an essential building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure and reactivity allow for the creation of diverse medicinal compounds with potential applications in treating various health conditions.
Used in Agrochemical Production:
In the agrochemical industry, ethyl 4-(2-bromoethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylate is utilized as a key intermediate in the synthesis of various agrochemicals. Its incorporation into these products enhances their effectiveness in agricultural applications, such as pest control and crop protection, ultimately contributing to increased crop yields and improved food security.
Used in the Synthesis of Fine Chemicals:
Ethyl 4-(2-bromoethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylate is also employed in the production of fine chemicals, which are high-purity chemicals used in various industries, including cosmetics, fragrances, and flavorings. Its versatile reactivity and functional groups enable the synthesis of a wide range of specialty chemicals with specific properties and applications.
Used as a Building Block for Organic Synthesis:
Due to its versatile reactivity and functional groups, ethyl 4-(2-bromoethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylate is used as a building block for the synthesis of various other organic compounds. This allows chemists to create new molecules with unique properties and potential applications in various fields, such as materials science, pharmaceuticals, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 220151-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,5 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220151-12:
(8*2)+(7*2)+(6*0)+(5*1)+(4*5)+(3*1)+(2*1)+(1*2)=62
62 % 10 = 2
So 220151-12-2 is a valid CAS Registry Number.
220151-12-2Relevant academic research and scientific papers
AMP deaminase inhibitors. 5. Design, synthesis, and SAR of a highly potent inhibitor series
Kasibhatla,Bookser,Xiao,Erion
, p. 613 - 618 (2007/10/03)
A highly potent AMP deaminase (AMPDA) inhibitor series was discovered by replacing the N3 substitutents of the two lead AMPDA inhibitor series with a conformationally restricted group. The most potent compound, 3-[2-(3-carboxy-4-bromo-5,6,7,8-tetrahydrona
Discovery of AMP mimetics that exhibit high inhibitory potency and specificity for AMP deaminase
Erion, Mark D.,Kasibhatla, Srinivas Rao,Bookser, Brett C.,Van Poelje, Paul D.,Reddy, M. Rami,Gruber, Harry E.,Appleman, James R.
, p. 308 - 319 (2007/10/03)
The first potent, specific, and cell-penetrable AMP deaminase (AMPDA) inhibitors were discovered through an investigation of 3-substituted 3,6,7,8-tetrahydroimidazo[4,5-d][1,3]diazepin-8-ol analogues. Inhibition constants for the most potent inhibitors we
