2445-98-9 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Ethylglutamic acid is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Organic Chemistry Reactions:
As a building block in organic chemistry, 3-Ethylglutamic acid is employed in a range of chemical reactions, facilitating the creation of diverse organic molecules with potential applications in various industries.
Used in Neuroscience and Neuropharmacology Research:
Due to its relationship with glutamic acid, a crucial component in neural signaling and transmission, 3-Ethylglutamic acid may have potential applications in the field of neuroscience and neuropharmacology. It could be instrumental in the study of neurological disorders and the development of treatments targeting neural pathways.
Used in Chemical Intermediates for Industrial Applications:
3-Ethylglutamic acid, with its unique properties, serves as a valuable chemical intermediate in various industrial applications, including the production of specialty chemicals, agrochemicals, and materials science products. Its versatility in chemical reactions makes it a sought-after component in the synthesis of complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 2445-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2445-98:
(6*2)+(5*4)+(4*4)+(3*5)+(2*9)+(1*8)=89
89 % 10 = 9
So 2445-98-9 is a valid CAS Registry Number.
2445-98-9Relevant academic research and scientific papers
Chemoenzymatic synthesis of glutamic acid analogues: Substrate specificity and synthetic applications of branched chain aminotransferase from Escherichia coli
Xian, Mo,Alaux, Sebastien,Sagot, Emmanuelle,Gefflaut, Thierry
, p. 7560 - 7566 (2008/03/11)
(Chemical Equation Presented) A new route to α-keto acids is described, based on the ozonolysis of enol acetates obtained from α-substituted β-keto esters. Escherichia coli branched chain aminotransferase (BCAT) activity toward a variety of substituted 2-oxoglutaric acids was demonstrated analytically. BCAT was shown to have a broad substrate spectrum, complementary to that of aspartate aminotransferase, and to offer access to a variety of glutamic acid analogues. The usefulness of BCAT was demonstrated through the synthesis of several 3- and 4-substituted derivatives.
A stereoselective synthesis of 3-substituted (S)-pyroglutamic and glutamic acids via OBO ester derivatives
Herdeis, Claus,Kelm, Bernd
, p. 217 - 229 (2007/10/03)
(S)-Pyroglutamic acid is transformed to the Cbz-protected 4-methyl-2,6,7-trioxabicyclo[2.2.2] octane (OBO) ester. This ortho ester functionality is employed as a bulky steering group for stereoselective introduction of alkyl and aryl groups via 1,4-cuprate addition to 3,4-unsaturated pyroglutamates. After deprotection and ringopening, 3-substituted glutamic acids are obtained.
Heterocyclic sulfonamide inhibitors of beta amyloid production
-
, (2008/06/13)
Compounds of Formula (I), wherein R1, R2, R3, R4, R5, R6, T, W, X, Y and Z are as defined herein are provided, together with pharmaceutically acceptable salt, hydrates and/or prodrugs there
