35891-72-6 Usage
Uses
Used in Organic Synthesis:
2-amino-4-methoxy-3-butenoic acid is used as a building block in organic synthesis for its potential to contribute to the creation of novel organic compounds. Its unique functional groups allow for versatile chemical reactions, facilitating the development of new molecules with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-amino-4-methoxy-3-butenoic acid is used as a starting material or intermediate in the development of new drugs. Its structural attributes may endow it with properties that are beneficial in medicinal chemistry, such as enhancing bioavailability, modulating pharmacokinetics, or targeting specific biological pathways.
While the specific applications and properties of 2-amino-4-methoxy-3-butenoic acid are still under investigation, its role in the chemical and pharmaceutical sectors is promising, with potential contributions to the advancement of both fields.
Check Digit Verification of cas no
The CAS Registry Mumber 35891-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,9 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35891-72:
(7*3)+(6*5)+(5*8)+(4*9)+(3*1)+(2*7)+(1*2)=146
146 % 10 = 6
So 35891-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO3/c1-9-3-2-4(6)5(7)8/h2-4H,6H2,1H3,(H,7,8)/b3-2+/t4-/m0/s1
35891-72-6Relevant academic research and scientific papers
Improved synthetic access to the β,γ-enol ether amino acids, L-2-amino-4-methoxy-trans-but-3-enoic acid and 1-2-amino-4-methoxy-cis-but-3-enoic acid
Alks, Vitauts,Sufrin, Janice R.
, p. 5257 - 5260 (2007/10/02)
A synthetic route to L-2-amino-4-methoxy-trans-but-3-enoic acid, exclusive of the cis-isomer, has been developed. The key step is direct formation of a trans-enol ether derivative from the corresponding dimethylacetal, by refluxing in CCl4, in the presence of hexamethyldisilazane and Me3SiI. The isomeric L-cis amino acid could be accessed from this route by isomerizing the intermediate, methyl DL-2-acetamido-2-amino-4-methoxy-trans-but-3-enoate at 217° C to give cis-trans mixture in a 1:10 ratio.
