3483-82-7 Usage
Description
Ethyl N-benzoyl-L-tyrosinate, also known as N-Benzoyl-L-tyrosine ethyl ester, is an L-tyrosine derivative that is the ethyl ester of N-benzoyltyrosine. It is a crystalline compound with unique chemical properties, making it a valuable substance for various applications.
Uses
Used in Research and Development:
Ethyl N-benzoyl-L-tyrosinate is used as a synthetic substrate for studying IMER (Intracellular Membrane-bound Esterase) systems. Its role in this application is to provide a controlled and specific compound for researchers to investigate the activity and function of IMER enzymes, which are crucial for understanding various biological processes.
Used in Pharmaceutical Industry:
Ethyl N-benzoyl-L-tyrosinate is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential applications in treating different diseases and conditions.
Used in Chemical Synthesis:
Ethyl N-benzoyl-L-tyrosinate is used as a building block in the chemical synthesis of various organic compounds. Its versatile structure makes it a valuable component in the creation of new molecules with specific properties and functions.
Used in Analytical Chemistry:
Ethyl N-benzoyl-L-tyrosinate is used as a reference compound in analytical chemistry for the calibration and validation of analytical methods and techniques. Its well-defined structure and properties make it an ideal candidate for ensuring the accuracy and reliability of experimental results.
Check Digit Verification of cas no
The CAS Registry Mumber 3483-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,8 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3483-82:
(6*3)+(5*4)+(4*8)+(3*3)+(2*8)+(1*2)=97
97 % 10 = 7
So 3483-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H19NO4/c1-2-23-18(22)16(12-13-8-10-15(20)11-9-13)19-17(21)14-6-4-3-5-7-14/h3-11,16,20H,2,12H2,1H3,(H,19,21)
3483-82-7Relevant articles and documents
Clickable coupling of carboxylic acids and amines at room temperature mediated by SO2F2: A significant breakthrough for the construction of amides and peptide linkages
Wang, Shi-Meng,Zhao, Chuang,Zhang, Xu,Qin, Hua-Li
supporting information, p. 4087 - 4101 (2019/04/30)
The construction of amide bonds and peptide linkages is one of the most fundamental transformations in all life processes and organic synthesis. The synthesis of structurally ubiquitous amide motifs is essential in the assembly of numerous important molecules such as peptides, proteins, alkaloids, pharmaceutical agents, polymers, ligands and agrochemicals. A method of SO2F2-mediated direct clickable coupling of carboxylic acids with amines was developed for the synthesis of a broad scope of amides in a simple, mild, highly efficient, robust and practical manner (>110 examples, >90% yields in most cases). The direct click reactions of acids and amines on a gram scale are also demonstrated using an extremely easy work-up and purification process of washing with 1 M aqueous HCl to provide the desired amides in greater than 99% purity and excellent yields.
Chromatographic Resolutions of Racemates, XI. Comparison of Optically Active Polyamides and Cellulose Triacetate
Blaschke, Gottfried,Kraft, Horst Peter,Markgraf, Hildegunde
, p. 3611 - 3617 (2007/10/02)
On optically active polyacrylic and polymethacrylic amides (1a-e) as well as on microcrystalline cellulose triacetate (2), numerous racemates including drugs are separated at least partially, the amide 4f completely on cellulose triacetate.By repeated chromatography on the polyamide 1a, (+)- and (-)-mandelic acid (4a) and (+)-hexobarbital (9d) also were obtained optically pure.
