CAS 5623-90-5

2-Oxaspiro[4.4]nonane-1,3-dione

Description:

2-Oxaspiro[4.4]nonane-1,3-dione, with the CAS number 5623-90-5, is a bicyclic organic compound characterized by its unique spiro structure, which consists of a nonane framework with a dione functional group and an ether linkage. This compound features a spiro carbon atom that connects two rings, contributing to its rigidity and distinct three-dimensional shape. The presence of the two carbonyl (C=O) groups in the 1 and 3 positions of the nonane ring enhances its reactivity, making it a potential candidate for various chemical transformations. The ether oxygen in the structure also plays a role in influencing its solubility and polarity. Typically, compounds like 2-Oxaspiro[4.4]nonane-1,3-dione may exhibit interesting biological activities and can be utilized in synthetic organic chemistry for the development of more complex molecules. Its unique structural features make it a subject of interest in both academic research and potential industrial applications.

Formula: C₈H₁₀O₃

InChI: InChI=1S/C8H10O3/c9-6-5-8(7(10)11-6)3-1-2-4-8/h1-5H2

InChI key: InChIKey=HOKKSYPZFBKQAZ-UHFFFAOYSA-N

SMILES: O=C1C2(CC(=O)O1)CCCC2

Synonyms:

• Cyclopentaneacetic acid, 1-carboxy-, cyclic anhydride
• 2-Oxaspiro[4.4]nonane-1,3-dione

2-Oxaspiro[4.4]nonane-1,3-dione

CAS: 5623-90-5

2-Oxaspiro[4.4]nonane-1,3-dione

Formula: C₈H₁₀O₃

Purity: ≥95%

Color and Shape: white. low melting solid

Molecular weight: 154.16g/mol

Ref: 54-OR1319

2-Oxaspiro[4.4]nonane-1,3-dione

CAS: 5623-90-5

2-Oxaspiro[4.4]nonane-1,3-dione is a heterocycle that has been developed as a lead molecule for the treatment of cancer. It was discovered by researchers at the University of Illinois who were investigating the use of Friedel-Crafts reaction to synthesize triazoles. 2-Oxaspiro[4.4]nonane-1,3-dione has physicochemical parameters that make it ideal for pharmaceutical research and development. This molecule has been shown to have anti-inflammatory properties and can be used to focus on carbon bond synthesis in order to synthesize pyridazines and ketocarboxylic acid derivatives.

Formula: C₈H₁₀O₃

Purity: Min. 95%

Molecular weight: 154.16 g/mol

Ref: 3D-FAA62390