CAS 62009-47-6

2-Aminopropanediamide

Description:

2-Aminopropanediamide, also known by its IUPAC name, is a diamine compound characterized by the presence of two amino groups (-NH2) attached to a three-carbon propane backbone. This compound is typically a white crystalline solid at room temperature and is soluble in water due to its polar functional groups. Its molecular structure allows it to participate in various chemical reactions, including those typical of amines, such as nucleophilic substitutions and condensation reactions. 2-Aminopropanediamide can act as a chelating agent, forming complexes with metal ions, which makes it of interest in coordination chemistry and potential applications in materials science. Additionally, it may have implications in biological systems, as amines can influence biological activity and interactions. Safety data indicates that, like many amines, it should be handled with care due to potential irritant properties. Overall, 2-Aminopropanediamide is a versatile compound with applications in both industrial and research settings.

Formula: C₃H₇N₃O₂

InChI: InChI=1S/C3H7N3O2/c4-1(2(5)7)3(6)8/h1H,4H2,(H2,5,7)(H2,6,8)

InChI key: InChIKey=GFQBSQXXHYLABK-UHFFFAOYSA-N

SMILES: C(C(N)=O)(C(N)=O)N

Synonyms:

• 2-Aminomalonamide
• Aminomalonamide
• Malonamide, 2-amino-
• NSC 75208
• Propanediamide, 2-amino-
• 2-Aminopropanediamide

2-Aminopropanediamide

CAS: 62009-47-6

Formula: C₃H₇N₃O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 117.1066

Ref: IN-DA00ECCP

2-Aminomalonamide

CAS: 62009-47-6

2-Aminomalonamide

Formula: C₃H₇N₃O₂

Purity: 98%

Color and Shape: orange solid

Molecular weight: 117.11g/mol

Ref: 54-OR61428

2-Aminomalonamide

CAS: 62009-47-6

Formula: C₃H₇N₃O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 117.108

Ref: 10-F038570

Aminomalonamide

CAS: 62009-47-6

Aminomalonamide is a diphenyl ether compound that has been used as an immunosuppressant in the treatment of cancer. It is also an activator of AMPK, which may be responsible for its insulin-sensitizing effects. Aminomalonamide blocks the synthesis of amines from ammonia and other sources by competitive inhibition of the enzyme, amino acid decarboxylase. It is also an inhibitor of malonic acid synthetase and triazine synthetase, which are enzymes involved in the production of carcinogenic compounds. Aminomalonamide has shown anti-inflammatory properties and can inhibit influenza virus replication.

Formula: C₃H₇N₃O₂

Purity: Min. 95%

Color and Shape: Off-White Powder

Molecular weight: 117.11 g/mol

Ref: 3D-FA17771

Aminomalonamide

Controlled Product

CAS: 62009-47-6

Applications Reagent used in the synthesis of Imidazole derivatives.
References Prasad, J., et al.: Bioorg. Med. Chem., 6, 1707 (1998),

Formula: C₃H₇N₃O₂

Color and Shape: Neat

Molecular weight: 117.11

Ref: TR-A611795

Aminomalonamide-13C3

Controlled Product

CAS: 62009-47-6

Formula: C₃H₇N₃O₂

Color and Shape: Neat

Molecular weight: 120.085

Ref: TR-A611796