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1,8-dibenzyl-1,8-diazaspiro[4.5]decan-3-ol
$550.00
CAS No.: NA
Catalog No.: 195313
Purity: 95%
MF: C22H28N2O
MW: 336.479
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1CC(CC12CCN(CC2)CC2=CC=CC=C2)O
Catalog No.: 195313
Purity: 95%
MF: C22H28N2O
MW: 336.479
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1CC(CC12CCN(CC2)CC2=CC=CC=C2)O
1,8-dibenzyl-1,8-diazaspiro[4.5]decan-3-ol; 1,8-dibenzyl-1,8-diazaspiro[4.5]decan-3-ol. PROPERTIES: 1,8-dibenzyl-1,8-diazaspiro[4.5]decan-3-ol appears as a colorless to pale yellow liquid with a slight odor. Its molecular formula is C20H26N2O, corresponding to a molecular weight of approximately 322.44 g/mol. The compound exhibits a boiling point around 200-205 C at 760 mmHg and a density of about 1.05 g/cm? at 25 C. It demonstrates moderate solubility in common organic solvents such as toluene, hexane, and diethyl ether but is sparingly soluble in water. The substance is sensitive to strong acids and bases, which may cause degradation. Proper storage requires keeping it in a tightly sealed, amber glass container in a cool, dry location away from direct sunlight and heat sources. The temperature should be maintained below 10 C if possible. Safety precautions include using chemical-resistant gloves, safety goggles, and lab coats to prevent skin absorption and inhalation of vapors. The compound may cause skin and eye irritation, and accidental ingestion may be harmful. In case of exposure, immediate rinsing with water and medical consultation is recommended. APPLICATIONS: 1,8-dibenzyl-1,8-diazaspiro[4.5]decan-3-ol serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly in the preparation of certain antidepressants and antipsychotics. Its spirocycle and benzyl groups provide structural features important for receptor binding and bioactivity. In materials science, it functions as a building block for creating chiral ligands and catalysts used in asymmetric synthesis. Additionally, it finds application in the development of fluorescent probes for bioimaging, where its spirocycle and hydroxyl groups allow for selective labeling of biological targets. The compound is also employed in the synthesis of agrochemicals, though specific applications in this area are limited to non-agricultural research settings.
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