61837-46-5 Usage
Description
2-Bromo-4-methylpentanoic Acid Methyl Ester is an organic compound that features a bromo and methyl group substitution on a pentanoic acid backbone, with an ester functional group derived from methyl alcohol. This molecule is known for its synthetic utility in the creation of various amino acids and other complex organic molecules.
Uses
Used in Pharmaceutical Industry:
2-Bromo-4-methylpentanoic Acid Methyl Ester is used as a synthetic intermediate for the production of a series of amino acids. Its application is particularly relevant in the pharmaceutical industry, where these amino acids can be used as building blocks for the development of new drugs or the modification of existing ones to improve their efficacy, bioavailability, or reduce side effects.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Bromo-4-methylpentanoic Acid Methyl Ester serves as a versatile reagent that can be employed in the creation of a wide range of organic compounds. Its unique structural features make it a valuable component in the synthesis of complex molecules, including those with potential applications in materials science, agrochemicals, and other specialty chemicals.
Used in Research and Development:
2-Bromo-4-methylpentanoic Acid Methyl Ester is also utilized in research and development settings, where it can be explored for its potential in creating novel compounds with specific biological activities or material properties. Its use in this context is driven by the need for new and innovative molecules to address various challenges in science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 61837-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,3 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61837-46:
(7*6)+(6*1)+(5*8)+(4*3)+(3*7)+(2*4)+(1*6)=135
135 % 10 = 5
So 61837-46-5 is a valid CAS Registry Number.
61837-46-5Relevant articles and documents
Enantioselective Synthesis of Quaternary α-Amino Acids Enabled by the Versatility of the Phenylselenonyl Group
Clemenceau, Antonin,Wang, Qian,Zhu, Jieping
supporting information, p. 18368 - 18372 (2016/12/16)
A novel Cinchona alkaloid-catalyzed enantioselective conjugate addition of α-alkyl substituted α-nitroacetates to phenyl vinyl selenone was developed. The resulting enantio-enriched α,α-dialkyl substituted α-nitroacetates were subsequently converted to various cyclic and acyclic quaternary α-amino acids, taking advantage of the rich functionalities of the resulting Michael adducts. Novel protocols allowing chemoselective reduction of phenyl selenone to phenyl selenide and reduction of alkyl phenyl selenones to alkanes are also reported.
ISATIN AND OXINDOLE COMPOUNDS
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Page/Page column 14, (2012/06/16)
Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of metabolic diseases and disorders such as, for example, type II diabetes mellitus.
PYRIDONE GLUCOKINASE ACTIVATORS
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Page/Page column 15, (2011/02/18)
Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful
