45214-91-3 Usage
Description
BOC-GLU(OME)-OH, also known as N-Boc-L-glutamic Acid 5-Methyl Ester, is an intermediate compound used in the synthesis of various organic compounds. It is characterized by the presence of a Boc-protected L-glutamic acid moiety and a 5-methyl ester group, which contribute to its unique chemical properties and reactivity.
Uses
Used in Pharmaceutical Industry:
BOC-GLU(OME)-OH is used as a synthetic intermediate for the production of Isodesmosine Chloride Hydrate (Synthetic) (I815051), a component of elastin. BOC-GLU(OME)-OH plays a crucial role in maintaining the elasticity and structural integrity of various tissues in the body.
Used in Chemical Synthesis:
BOC-GLU(OME)-OH is used as a building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for versatile synthetic routes and the formation of diverse molecular architectures.
Used in Research and Development:
BOC-GLU(OME)-OH serves as a valuable research tool for studying the properties and reactivity of Boc-protected amino acids and their derivatives. It can be used to investigate the effects of different protecting groups on the synthesis and stability of various organic compounds.
Due to its hygroscopic nature, BOC-GLU(OME)-OH must be stored over a desiccant, such as silica gel, to maintain its purity and stability. This ensures that the compound remains suitable for use in various applications, including the synthesis of Isodesmosine Chloride Hydrate and other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 45214-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,2,1 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 45214-91:
(7*4)+(6*5)+(5*2)+(4*1)+(3*4)+(2*9)+(1*1)=103
103 % 10 = 3
So 45214-91-3 is a valid CAS Registry Number.
45214-91-3Relevant articles and documents
A PROCESS FOR THE PREPARATION OF L-GLUTAMINE
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Page/Page column 14; 15, (2022/01/24)
The present invention relates to a process for the preparation of L-Glutamine of Formula (I). The present invention also relates to an improved process for the purification of L-Glutamine of Formula (I) having specific bulk density and Hausner ratio.
NOVEL JAK1 SELECTIVE INHIBITORS AND USES THEREOF
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Page/Page column 47, (2018/04/21)
The new 1H-furo[3,2-b]imidazo[4,5-d]pyridine derivatives are selective Jak1 kinase inhibitors useful in treating disorders related to Jak1 activities such as autoimmune diseases or disorders, inflammatory diseases or disorders, and cancer or neoplastic di
Synthesis of ortho-carboranyl derivatives of (S)-asparagine and (S)-glutamine
Gruzdev,Levit,Olshevskaya,Krasnov
, p. 769 - 776 (2017/07/07)
(S)-Asparagine and (S)-glutamine ortho-carboranyl derivatives with free amino and carboxy groups in the α-position were synthesized. By an example of Nγ-(1,2-dicarba-closo-dodecarboran-3-yl)-(S)-glutamine it was demonstrated that the developed synthetic approach carboranyl derivatives of amino acids allowed the preparation of optically pure isomers.