28544-45-8 Usage
Uses
Used in Pharmaceutical Research and Development:
(BENZOYL-METHYL-AMINO)-PHENYL-ACETIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for [application reason]. Its unique structure and properties make it a promising candidate for the development of new drugs to treat various medical conditions.
Used in Drug Synthesis:
In the pharmaceutical industry, (BENZOYL-METHYL-AMINO)-PHENYL-ACETIC ACID is used as a building block for the creation of novel drug molecules. Its chemical structure allows for further functionalization and modification, enabling the development of drugs with improved efficacy, selectivity, and safety profiles.
Used in Medicinal Chemistry:
(BENZOYL-METHYL-AMINO)-PHENYL-ACETIC ACID serves as a valuable compound in medicinal chemistry for [application reason]. Researchers can use (BENZOYL-METHYL-AMINO)-PHENYL-ACETIC ACID to study its interactions with biological targets, such as enzymes, receptors, or ion channels, to gain insights into its potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 28544-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,4 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28544-45:
(7*2)+(6*8)+(5*5)+(4*4)+(3*4)+(2*4)+(1*5)=128
128 % 10 = 8
So 28544-45-8 is a valid CAS Registry Number.
28544-45-8Relevant academic research and scientific papers
Synthesis, characterization and crystallographic studies of three 2-aryl-3-methyl-4-aryl-1,3-thiazolium-5-thiolates
De Athayde-Filho, Petronio Filgueiras,Miller, Joseph,Simas, Alfredo Mayall,Lira, Bruno Freitas,De Souza Luis, José Alixandre,Zuckerman-Schpector, Júlio
, p. 685 - 690 (2007/10/03)
Mesoionic 2,4-diphenyl-3-methyl-1,3-thiazolium-5-thiolate, 2-(4′-chlorophenyl)-3-methyl-4-phenyl-1,3-thiazolium-5-thiolate and 2-(4′-chlorophenyl)-3-methyl-4-(4′-isopropyl-phenyl)-1,3- thiazolium-5-thiolate were synthesized via N-methyl-C-aryl-glycines, i
Tandem 1,3-dipolar cycloadditions of muenchnones. Syntheses and molecular structures of 10-azatetracyclo[6.3.0.04,11.05,9]undecanes and azahomopentaprismane
Gribble, Gordon W.,Sponholtz III, William R.,Switzer, Frank L.,D'Amato, Ferdinando J.,Byrn, Marianne P.
, p. 993 - 994 (2007/10/03)
Photocyclization of 10-benzyl-9,11-diphenyl-10-azatetracyclo[6.3.0.04,11.0 5,9]undeca-2,6-diene 11, prepared in one step from muenchnone 7 and cycloocta-1,3,5,7-tetraene 10, gives azahomopentaprismane 12.
