CAS 3775-60-8

1,3,4-oxadiazol-2-amine

Description:

1,3,4-Oxadiazol-2-amine is a heterocyclic compound characterized by a five-membered ring containing two nitrogen atoms and three carbon atoms, with an amino group (-NH2) attached to the second carbon of the oxadiazole ring. This compound is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. It typically exhibits properties such as moderate solubility in polar solvents and stability under standard conditions. The presence of the amino group contributes to its reactivity, allowing for various chemical modifications. Additionally, 1,3,4-oxadiazol-2-amine can participate in hydrogen bonding, which may influence its interactions with biological targets. Its structural features make it a subject of interest in medicinal chemistry, particularly for the development of new therapeutic agents. As with many nitrogen-containing heterocycles, it may also exhibit interesting electronic properties, which can be leveraged in material science and organic synthesis.

Formula: C₂H₃N₃O

InChI: InChI=1/C2H3N3O/c3-2-5-4-1-6-2/h1H,(H2,3,5)

SMILES: c1n[nH]c(=N)o1

NSC45356

CAS: 3775-60-8

Formula: C₂H₃N₃O

Purity: 95%

Color and Shape: Solid

Molecular weight: 85.0647

Ref: IN-DA00CITH

1,3,4-oxadiazol-2-amine

CAS: 3775-60-8

1,3,4-oxadiazol-2-amine

Purity: 97%

Color and Shape: Solid

Molecular weight: 85.06g/mol

Ref: 54-OR54600

1,3,4-Oxadiazol-2-amine

CAS: 3775-60-8

Formula: C₂H₃N₃O

Color and Shape: Neat

Molecular weight: 85.06

Ref: TR-E590025

1,3,4-oxadiazol-2-amine

CAS: 3775-60-8

Formula: C₂H₃N₃O

Purity: 95%

Color and Shape: Solid

Molecular weight: 85.066

Ref: 10-F313185

1,3,4-Oxadiazol-2-amine

CAS: 3775-60-8

1,3,4-Oxadiazol-2-amine is a synthetic compound that belongs to the group of peptidomimetics. It is an alkylating agent that has been shown to inhibit glycogen synthase kinase 3 (GSK3) and prevent the formation of amyloid plaques in Alzheimer's disease. 1,3,4-Oxadiazol-2-amine also has antibacterial activity against Gram-positive and Gram-negative bacteria. This compound can be synthesized by reacting chloroacetaldehyde with 2-(2'-aminophenoxy)ethanol in the presence of acid. The molecular weight for this compound is 167.260 g/mol. Crystals are obtained from melting the substance at 180 °C under vacuum and then allowing it to cool down to room temperature over a period of 4 hours. The crystal system for this molecule is monoclinic and its space group is P21/c. X-ray diffraction

Formula: C₂H₃N₃O

Purity: Min. 95%

Molecular weight: 85.06 g/mol

Ref: 3D-FO135962