CAS 7788-14-9

1,2,4-Oxadiazol-3-amine,5-phenyl-

Description:

1,2,4-Oxadiazol-3-amine, 5-phenyl- (CAS 7788-14-9) is a heterocyclic organic compound characterized by the presence of an oxadiazole ring, which consists of two nitrogen atoms and three carbon atoms in its five-membered structure. This compound features an amino group (-NH2) at the 3-position and a phenyl group at the 5-position of the oxadiazole ring, contributing to its chemical reactivity and potential applications. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. The presence of both the amino and phenyl groups allows for various chemical modifications, making it a candidate for use in pharmaceuticals, agrochemicals, and materials science. Additionally, compounds of this class may exhibit biological activity, including antimicrobial or anti-inflammatory properties, although specific biological data would depend on empirical studies. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, enhancing its utility in synthetic chemistry.

Formula: C₈H₇N₃O

Synonyms:

• 1,2,4-Oxadiazole,3-amino-5-phenyl- (7CI,8CI)
• 3-Amino-5-phenyl-1,2,4-oxadiazole

1,2,4-Oxadiazol-3-amine,5-phenyl-

CAS: 7788-14-9

Formula: C₈H₇N₃O

Purity: %

Color and Shape: Solid

Molecular weight: 161.1607

Ref: IN-DA005EQQ

5-Phenyl-1,2,4-oxadiazol-3-amine

CAS: 7788-14-9

5-Phenyl-1,2,4-oxadiazol-3-amine

Purity: 95%

Molecular weight: 161.16g/mol

Ref: 54-OR939721

5-Phenyl-1,2,4-oxadiazol-3-amine

CAS: 7788-14-9

Formula: C₈H₇N₃O

Purity: 95+%

Color and Shape: Crystalline,Powder

Molecular weight: 161.164

Ref: 10-F064952

5-Phenyl-1,2,4-oxadiazol-3-amine

Controlled Product

CAS: 7788-14-9

Formula: C₈H₇N₃O

Color and Shape: Neat

Molecular weight: 161.16

Ref: TR-P400158

5-Phenyl-1,2,4-oxadiazol-3-amine

CAS: 7788-14-9

5-Phenyl-1,2,4-oxadiazol-3-amine is a trifluoromethylated and fluorinated analog of oxadiazole. It has been shown to have hydrolysis and condensation properties, which can be used to target a variety of enzymes. In particular, 5-phenyl-1,2,4-oxadiazol-3-amine binds to the active site of the enzyme protein kinase C (PKC) by hydrophobic interactions. The PKC is an enzyme that plays a key role in the production of proteins involved in inflammatory responses. The PKC enzyme complex is activated by the binding of calcium ions and this activation leads to an increase in phosphorylation events. This causes the cells to become more sensitive to inflammatory stimuli. 5-phenyl-1,2,4-oxadiazol-3-amine has been shown to inhibit PKC activity by interfering with calcium ion

Formula: C₈H₇N₃O

Purity: Min. 95%

Molecular weight: 161.16 g/mol

Ref: 3D-FP127174