196394-48-6 Usage
Description
METHYL (2S,4S)-1-(TERT-BUTOXYCARBONYL)-4-METHYLPYROGLUTAMATE, with the CAS number 196394-48-6, is a compound that is characterized as a light yellow oil. It is primarily utilized in the field of organic synthesis, playing a crucial role in the creation of various chemical compounds and materials.
Uses
Used in Organic Synthesis:
METHYL (2S,4S)-1-(TERT-BUTOXYCARBONYL)-4-METHYLPYROGLUTAMATE is used as a synthetic building block for the development of new organic compounds. Its unique structure allows it to be a valuable component in the synthesis of complex molecules, contributing to the advancement of chemical research and innovation.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, METHYL (2S,4S)-1-(TERT-BUTOXYCARBONYL)-4-METHYLPYROGLUTAMATE is used as an intermediate in the synthesis of various drugs. Its versatility in organic synthesis makes it a valuable asset in the development of new medications, potentially leading to the creation of novel treatments for a wide range of medical conditions.
Used in Chemical Research:
METHYL (2S,4S)-1-(TERT-BUTOXYCARBONYL)-4-METHYLPYROGLUTAMATE is also employed in chemical research as a tool to study the properties and behavior of different organic compounds. Its light yellow oil form and unique chemical structure make it an interesting subject for further investigation, potentially leading to new discoveries and insights in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 196394-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,3,9 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 196394-48:
(8*1)+(7*9)+(6*6)+(5*3)+(4*9)+(3*4)+(2*4)+(1*8)=186
186 % 10 = 6
So 196394-48-6 is a valid CAS Registry Number.
196394-48-6Relevant articles and documents
Chemoselective Intramolecular Functionalization of Methyl Groups in Nonconstrained Molecules Promoted by N-Iodosulfonamides
Paz, Nieves R.,Rodríguez-Sosa, Dionisio,Valdés, Haydee,Marticorena, Ricardo,Melián, Daniel,Copano, M. Belén,González, Concepción C.,Herrera, Antonio J.
supporting information, p. 2370 - 2373 (2015/06/02)
Mechanistic evidence observed in Hofmann-L?ffler-Freytag-type reactions has been crucial to achieve the chemoselective functionalization of methyl groups under mild conditions. Radical-mediated methyl iodination and subsequent oxidative deiodination are the key steps in this functionalization, where iodine chemistry has a pivotal role on the formation of the C-N bond. The concepts of single hydrogen atom transfer (SHAT) and multiple hydrogen atom transfer (MHAT) are introduced to describe the observed chemoselectivity. (Chemical Equation Presented).
Malate salts, and polymorphs of (3S,5S)-7-[3-amino-5-methyl-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid
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Page/Page column 5, (2008/06/13)
The present invention is directed to malate salts of (3S,5S)-7-[3-amino-5-methyl-piperidinyl]-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid, and its polymorphs. The present invention is also directed to pharmaceutical compositions comprising the described salts and polymorphs.
Coupling process for preparing quinolone intermediates
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Page/Page column 4; 5, (2008/06/13)
Process for making 7-cycloamino-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acids. Borate ester compounds suitable for use in such process.
