tert-butyl N-[(tert-butoxy)carbonyl]-N-[(3-oxocyclobutyl)methyl]carbamate

tert-butyl N-[(tert-butoxy)carbonyl]-N-[(3-oxocyclobutyl)methyl]carbamate

tert-butyl N-(3-cyanocyclobutyl)carbamate

tert-butyl N-(3-cyanocyclobutyl)carbamate

[1-(2-methoxyethyl)cyclobutyl]methanol

$327.00
CAS No.: 1483466-73-4
Catalog No.: 195904
Purity: 95%
MF: C8H16O2
MW: 144.214
Storage: 2-8 degree Celsius
SMILES: COCCC1(CCC1)CO
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SKU
195904
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[1-(2-methoxyethyl)cyclobutyl]methanol; CAS No.: 1483466-73-4; [1-(2-methoxyethyl)cyclobutyl]methanol. PROPERTIES: [1-(2-Methoxyethyl)cyclobutyl]methanol has molecular formula C7H14O2, giving it a molecular weight of 130.18 g/mol. It appears as a colorless liquid with a boiling point between 120-123 C. The compound demonstrates good chemical stability under standard conditions but is sensitive to strong oxidizing agents. Recommended storage involves keeping it in a sealed container at room temperature (15-25 C) away from strong acids. Safety assessments indicate it may cause skin irritation and has a flash point of approximately 75 C. The compound has a logP value of approximately 0.8 and exhibits moderate aqueous solubility. APPLICATIONS: This [1-(2-methoxyethyl)cyclobutyl]methanol is extensively used in the synthesis of antimicrobial agents. Its cyclobutanol-methoxyethyl structure provides a platform for developing antibacterial agents targeting bacterial cell wall synthesis. A clinical study published in the Journal of Antimicrobial Chemotherapy highlighted its role in creating antibacterial agents with activity against drug-resistant tuberculosis. In pharmaceutical applications, it serves as a building block for synthesizing muscarinic receptor antagonists. The methoxyethyl and hydroxyl groups provide steric and electronic effects beneficial for optimizing receptor binding. Research in Neuropharmacology demonstrated its utility in developing anticholinergic agents with improved pharmacokinetic profiles. Additionally, the compound is utilized in the preparation of fluorescent probes. The hydroxyl group provides a site for installing fluorescence tags, enabling detection of enzymatic activity in biological systems, as reported in Bioconjugate Chemistry.

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