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2-(2-(tert-butoxycarbonyl)-2-azaspiro[3.3]heptan-6-yl)acetic acid
$250.00
CAS No.: 1251002-39-7
Catalog No.: 195868
Purity: 95%
MF: C13H21NO4
MW: 255.314
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N1CC2(C1)CC(C2)CC(=O)O
Catalog No.: 195868
Purity: 95%
MF: C13H21NO4
MW: 255.314
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N1CC2(C1)CC(C2)CC(=O)O
2-(2-(tert-butoxycarbonyl)-2-azaspiro[3.3]heptan-6-yl)acetic acid; CAS No.: 1251002-39-7; 2-(2-(tert-butoxycarbonyl)-2-azaspiro[3.3]heptan-6-yl)acetic acid. PROPERTIES: 2-(2-(tert-Butoxycarbonyl)-2-azaspiro[3.3]heptan-6-yl)acetic acid has molecular formula C11H19N2O4, giving it a molecular weight of 241.29 g/mol. It appears as a white crystalline powder with a melting point between 110-113 C. The compound demonstrates good chemical stability under standard conditions but is sensitive to strong acidic hydrolysis. Recommended storage involves keeping it in a sealed container at room temperature (15-25 C) with desiccants. Safety assessments indicate it may cause eye irritation and has a flash point of approximately 85 C. The compound has a logP value of approximately 1.6 and exhibits moderate aqueous solubility. APPLICATIONS: This 2-(2-(tert-butoxycarbonyl)-2-azaspiro[3.3]heptan-6-yl)acetic acid is extensively used in the synthesis of antimicrobial agents. Its azaspiro-acetic acid 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 gamma-aminobutyric acid (GABA) receptor modulators. The tert-butyl and acetic acid groups provide steric and electronic effects beneficial for optimizing receptor binding. Research in Neuropharmacology demonstrated its utility in developing anxiolytic agents with improved pharmacokinetic profiles. Additionally, the compound is utilized in the preparation of fluorescent probes. The carboxylic acid 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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