CAS 50479-22-6
:Butanoic acid, 4-amino-, 1,1-dimethylethyl ester
Description:
Butanoic acid, 4-amino-, 1,1-dimethylethyl ester, also known by its CAS number 50479-22-6, is an organic compound characterized by its ester functional group derived from butanoic acid and an amino group. This compound typically exhibits a moderate polarity due to the presence of both the ester and amino functionalities, which can influence its solubility in various solvents. It is likely to be a colorless to pale yellow liquid or solid, depending on its specific form and purity. The presence of the amino group suggests potential for hydrogen bonding, which can affect its reactivity and interactions with other molecules. This compound may be used in various applications, including pharmaceuticals and agrochemicals, due to its potential biological activity. Additionally, its structure indicates that it may participate in reactions typical of esters and amines, such as hydrolysis or amine substitution. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C8H17NO2
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Found 4 products.
tert-butyl 4-aminobutanoate
CAS:Formula:C8H17NO2Purity:97%Color and Shape:LiquidMolecular weight:159.2261tert-Butyl 4-aminobutanoate
CAS:<p>tert-Butyl 4-aminobutanoate</p>Formula:C8H17NO2Purity:97%Color and Shape: colourless liquidMolecular weight:159.23g/moltert-Butyl 4-aminobutanoate
CAS:<p>tert-Butyl 4-aminobutanoate is an amine that has been shown to stabilize the natural formyl group of the molecule. It is a nucleophilic reactant, which means it will react with electrophiles. The nucleophilic attack occurs when a nucleophile reacts with an electrophile, leading to the formation of a new bond between the two molecules. Tert-butyl 4-aminobutanoate also has a hydroxymethyl group on its side chain. This hydroxymethyl group can be reduced by pyridoxal phosphate in order to form gamma-aminobutyric acid.</p>Formula:C8H17NO2Purity:Min. 95%Molecular weight:159.23 g/mol
