CAS 2819-56-9

2-Oxo-1-oxaspiro[4.5]decane-4-carboxylic acid

Description:

2-Oxo-1-oxaspiro[4.5]decane-4-carboxylic acid, with the CAS number 2819-56-9, is a bicyclic compound characterized by its unique spiro structure, which consists of a fused ring system. This compound features a carboxylic acid functional group, contributing to its acidity and potential reactivity. The presence of the oxo group indicates a carbonyl functionality, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The spiro configuration introduces strain and rigidity to the molecule, influencing its physical and chemical properties. Typically, compounds like this may exhibit interesting biological activities, making them of interest in medicinal chemistry and drug design. Additionally, the compound's solubility, stability, and reactivity can be affected by the surrounding functional groups and the overall molecular structure. As with many organic compounds, its behavior in different solvents and under various conditions can provide insights into its potential applications in synthesis and material science.

Formula: C₁₀H₁₄O₄

InChI: InChI=1/C10H14O4/c11-8-6-7(9(12)13)10(14-8)4-2-1-3-5-10/h7H,1-6H2,(H,12,13)

InChI key: InChIKey=ZTXZIBLPLHQZAQ-UHFFFAOYSA-N

SMILES: C(O)(=O)C1C2(OC(=O)C1)CCCCC2

Synonyms:

• 1-Oxaspiro[4.5]decane-4-carboxylic acid, 2-oxo-
• Butanedioic acid, (1-hydroxycyclohexyl)-, γ-lactone
• Cyclohexanesuccinic acid, 1-hydroxy-, γ-lactone
• NSC 25328
• 2-Oxo-1-oxaspiro[4.5]decane-4-carboxylic acid
• 2-Oxo-1-oxaspiro[4.5]decane-4-carboxylic acid
• TOSLAB 868773
• 2-OXO-1-OXA-SPIRO[4.5]DECANE-4-CARBOXYLIC ACID
• 2-keto-1-oxaspiro[4.5]decane-4-carboxylic acid
• 3-OXO-4-OXASPIRO[4.5]DECANE-1-CARBOXYLIC ACID
• CHEMBRDG-BB 4004219

2-Oxo-1-oxaspiro[4.5]decane-4-carboxylic acid

CAS: 2819-56-9

Formula: C₁₀H₁₄O₄

Molecular weight: 198.2158

Ref: IN-DA007L7I

2-Oxo-1-oxaspiro[4.5]decane-4-carboxylic acid

CAS: 2819-56-9

2-Oxo-1-oxaspiro[4.5]decane-4-carboxylic acid is a nitrile that can be synthesized by decarboxylation of 4-chloro-2,6-dimethylaniline with nitrous acid and sulfuric acid. The intramolecular cyclization of methyl 2-(nitrobenzyl)malonate to the thiazole ring is catalyzed by a mixture of acetic anhydride and pyridine. The reaction is carried out at refluxing temperatures in a homogeneous solvent such as toluene or chloroform. This product can also be obtained from the reaction of 2,6-dimethylaniline with hydroxylamine hydrochloride in the presence of sodium hydroxide.

Formula: C₁₀H₁₄O₄

Purity: Min. 95%

Molecular weight: 198.22 g/mol

Ref: 3D-CAA81956