127358-24-1 Usage
Description
(R)-AMINO-FURAN-2-YL-ACETIC ACID METHYL ESTER, with the molecular formula C7H9NO3, is a chemical compound that is an ester derivative of amino-furan-2-yl-acetic acid. It features a furan ring and an amino group, which contribute to its potential utility in various chemical reactions and as a building block for synthesizing other compounds. The presence of a methyl ester group enhances its reactivity and solubility, making it a versatile chemical with applications in chemistry and drug development.
Uses
Used in Organic Synthesis:
(R)-AMINO-FURAN-2-YL-ACETIC ACID METHYL ESTER is used as a key intermediate in organic synthesis for the production of various complex molecules and pharmaceutical compounds. Its unique structural features, including the furan ring and amino group, facilitate its involvement in a wide range of chemical reactions, making it a valuable component in the synthesis process.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (R)-AMINO-FURAN-2-YL-ACETIC ACID METHYL ESTER is used as a building block for the development of new drugs. Its structural properties allow it to be a potential candidate for the creation of novel therapeutic agents, particularly in the areas of medicinal chemistry and drug design. (R)-AMINO-FURAN-2-YL-ACETIC ACID METHYL ESTER's reactivity and solubility, due to the methyl ester group, further enhance its applicability in drug development.
Used in Chemical Reactions:
(R)-AMINO-FURAN-2-YL-ACETIC ACID METHYL ESTER is utilized as a reactant in various chemical reactions, such as esterification, amidation, and substitution reactions. Its furan ring and amino group provide opportunities for functional group transformations and the formation of new chemical entities, contributing to the advancement of chemical research and innovation.
Overall, (R)-AMINO-FURAN-2-YL-ACETIC ACID METHYL ESTER is a multifaceted chemical compound with a broad spectrum of applications in organic synthesis, pharmaceutical research, and chemical reactions, showcasing its significance in the fields of chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 127358-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,5 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127358-24:
(8*1)+(7*2)+(6*7)+(5*3)+(4*5)+(3*8)+(2*2)+(1*4)=131
131 % 10 = 1
So 127358-24-1 is a valid CAS Registry Number.
127358-24-1Relevant articles and documents
Asymmetric synthesis of arylglycines
Williams,Hendrix
, p. 3723 - 3727 (2007/10/02)
The asymmetric synthesis of several arylglycines are reported. The methodology deployed involves either cuprate or Friedel - Crafts couplings to chiral bromoglycinates. The % ee's range from 82 to 94%. Both an oxidative and reductive protocol are employed to unmask the oxazinone chiral auxilliary providing the free α-amino acids.
