(R)-(1,4-dioxan-2-yl)-N-methylmethanamine hydrochloride

(R)-(1,4-dioxan-2-yl)-N-methylmethanamine hydrochloride

(1,4-dioxan-2-yl)methanamine

(1,4-dioxan-2-yl)methanamine

5-hydrazono-2,2-dimethyl-1,3-dioxane-4,6-dione

$350.00
CAS No.: 7270-63-5
Catalog No.: 196238
Purity: 95%
MF: C6H8N2O4
MW: 172.14
Storage: 2-8 degree Celsius
SMILES: N(N)=C1C(OC(OC1=O)(C)C)=O
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196238
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5-hydrazono-2,2-dimethyl-1,3-dioxane-4,6-dione; CAS No.: 7270-63-5; 5-hydrazono-2,2-dimethyl-1,3-dioxane-4,6-dione. PROPERTIES: This compound presents a 5-hydrazono-2,2-dimethyl-1,3-dioxane-4,6-dione structure, combining a hydrazono group and a dimethyl-substituted 1,3-dioxane-4,6-dione framework. It typically appears as a white to off-white crystalline solid with a molecular weight of approximately 182.1 g/mol (C5H8N2O4). The melting point ranges between 180-185 C, and it exhibits moderate solubility in common organic solvents like ethanol, methanol, and DMSO while being sparingly soluble in water. Proper storage requires a tightly sealed container in a cool, dry place. Safety considerations include wearing appropriate PPE. It is classified as a skin and eye irritant (GHS07) with the hazard statement H315-H319. APPLICATIONS: 5-Hydrazono-2,2-dimethyl-1,3-dioxane-4,6-dione serves as a specialized intermediate in pharmaceutical research. Its 5-hydrazono-2,2-dimethyl-1,3-dioxane-4,6-dione structure enables participation in various reactions, including nucleophilic substitution at the hydrazono group and electrophilic substitution at the dioxane ring. In medicinal chemistry, it is used to develop bioactive molecules targeting kinases, proteases, and G protein-coupled receptors. The hydrazono group can undergo reduction to hydrazine or condensation reactions to form hydrazones. This compound also functions as a building block in the synthesis of fluorescent dyes and bioconjugation reagents. Academic studies utilize it as a model system in Medicinal Chemistry journals, focusing on optimizing the 5-hydrazono-2,2-dimethyl-1,3-dioxane-4,6-dione scaffold for improved biological activity and target engagement.

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