150368-37-9 Usage
Uses
Used in Chemical Reactions:
2-Amino-6-Fluoro-3-Nitrobenzoic Acid Ethyl Ester is used as a chemical intermediate for various chemical reactions in laboratory or industrial settings. Its functional groups, such as amine, fluoride, and nitro, contribute to its reactivity and make it a valuable compound for synthesis and modification of other chemicals.
Used in Pharmaceutical Industry:
2-Amino-6-Fluoro-3-Nitrobenzoic Acid Ethyl Ester is used as a building block in the synthesis of pharmaceutical compounds. Its unique structure and functional groups can be utilized to create new drug molecules with potential therapeutic applications.
Used in Material Science:
2-Amino-6-Fluoro-3-Nitrobenzoic Acid Ethyl Ester is used as a component in the development of new materials with specific properties. Its chemical structure can be incorporated into polymers or other materials to enhance their characteristics, such as stability, reactivity, or functionality.
Used in Research and Development:
2-Amino-6-Fluoro-3-Nitrobenzoic Acid Ethyl Ester is used as a research compound for studying its properties and potential applications. Scientists and researchers can explore its reactivity, interactions with other chemicals, and its potential uses in various fields, such as medicine, material science, or environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 150368-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,3,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 150368-37:
(8*1)+(7*5)+(6*0)+(5*3)+(4*6)+(3*8)+(2*3)+(1*7)=119
119 % 10 = 9
So 150368-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9FN2O4/c1-2-16-9(13)7-5(10)3-4-6(8(7)11)12(14)15/h3-4H,2,11H2,1H3
150368-37-9Relevant academic research and scientific papers
Quinoxaline biphenyl angiotensin II inhibitors
-
, (2008/06/13)
Angiotensin II inhibition is exhibited by STR1 wherein: X is --CH2 -- or O; R is hydrogen, alkyl, aryl, cycloalkyl, aralkyl, or cycloalkylalkyl; R1 and R2 are each independently O or absent; R3 is hydrogen, alkyl, alkenyl, alkoxy, cycloalkyl, aryl, aralkyl, cycloalkylalkyl, halo, haloalkyl, or haloalkoxy; R4 is hydrogen, alkyl, alkenyl, alkoxy, aryl, cycloalkyl, aralkyl, cycloalkylalkyl, --R8 --OH, or --R8 CO2 R9 ; and the remaining symbols are as defined in the specification.
Quinoxaline N-oxide containing potent angiotensin II receptor antagonists: Synthesis, biological properties, and structure-activity relationships
Kyoung Soon Kim,Qian,Bird,Dickinson,Moreland,Schaeffer,Waldron,Delaney,Weller,Miller
, p. 2335 - 2342 (2007/10/02)
A series of novel quinoxaline heterocycle containing angiotensin II receptor antagonist analogs were prepared. This heterocycle was coupled to the biphenyl moiety via an oxygen atom linker instead of a carbon atom. Many of these analogs exhibit very poten
