CAS 53171-39-4

methyl 4-amino-4-oxobutanoate

Description:

Methyl 4-amino-4-oxobutanoate, with the CAS number 53171-39-4, is an organic compound characterized by its structure, which includes a methyl ester group, an amino group, and a ketone functional group. This compound typically appears as a white to off-white solid or crystalline substance. It is soluble in polar solvents such as water and alcohols, which is indicative of its polar functional groups. The presence of the amino group suggests that it may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Methyl 4-amino-4-oxobutanoate can serve as an intermediate in the synthesis of pharmaceuticals and other organic compounds, particularly in the development of amino acids and related derivatives. Its reactivity and functional groups make it a valuable compound in organic synthesis and medicinal chemistry. As with many organic compounds, proper handling and safety precautions should be observed, as it may pose health risks if ingested or inhaled.

Formula: C₅H₉NO₃

InChI: InChI=1/C5H9NO3/c1-9-5(8)3-2-4(6)7/h2-3H2,1H3,(H2,6,7)

SMILES: COC(=O)CCC(=N)O

Synonyms:

• Butanoic Acid, 4-Amino-4-Oxo-, Methyl Ester

Methyl Succinamate

CAS: 53171-39-4

Formula: C₅H₉NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 131.1299

Ref: IN-DA003594

Methyl Succinamate

CAS: 53171-39-4

Methyl Succinamate

Formula: C₅H₉NO₃

Purity: 98%

Color and Shape: white solid

Molecular weight: 131.13g/mol

Ref: 54-OR919943

Methyl 4-amino-4-oxobutanoate

CAS: 53171-39-4

Purity: 97%

Molecular weight: 131.1309967

Ref: 10-F774391

Methyl Succinamate

CAS: 53171-39-4

Methyl succinate is a heterocyclic compound that has been shown to be effective in the treatment of autoimmune diseases. It has also been shown to inhibit cancer cells, as well as infectious diseases. Methyl Succinamate is an amide and intramolecular hydrogen bond donor. This chemical ionization technique can be used for the specific determination of this compound in biological fluids such as blood plasma or serum. The NMR spectra of methyl succinate are consistent with its structure, which consists of an amide group and three methyl groups. Methyl succinate binds to the bradykinin B2 receptor and inhibits its activity by blocking the binding site.

Formula: C₅H₉NO₃

Purity: Min. 95%

Molecular weight: 131.13 g/mol

Ref: 3D-DCA17139

Methyl Succinamate

CAS: 53171-39-4

Formula: C₅H₉NO₃

Purity: >98.0%(GC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 131.13

Ref: 3B-S0479