CAS 25021-04-9
:Acetic acid,2-cyclobutylidene-
Description:
Acetic acid, 2-cyclobutylidene- (CAS 25021-04-9) is an organic compound characterized by the presence of both acetic acid and a cyclobutylidene group. This substance features a cyclobutane ring, which is a four-membered carbon ring, contributing to its unique structural properties. The presence of the acetic acid moiety indicates that it has a carboxylic acid functional group, which imparts acidic characteristics and the ability to participate in various chemical reactions, such as esterification and neutralization. The cyclobutylidene group can influence the compound's reactivity and stability, potentially affecting its physical properties like boiling and melting points. Generally, compounds with such structures may exhibit interesting biological activities and can be utilized in various synthetic applications. However, specific data regarding its solubility, volatility, and toxicity would require further investigation or reference to specialized chemical databases. Overall, acetic acid, 2-cyclobutylidene- represents a unique intersection of cyclic and acyclic chemistry, making it a subject of interest in organic synthesis and chemical research.
Formula:C6H8O2
Synonyms:- Aceticacid, cyclobutylidene- (9CI)
- D1,a-Cyclobutaneacetic acid(6CI,8CI)
- D1'a-Cyclobutaneacetic acid (7CI)
- Cyclobutylideneaceticacid
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Found 4 products.
2-cyclobutylideneacetic acid
CAS:Formula:C6H8O2Purity:98%Color and Shape:SolidMolecular weight:112.12652-Cyclobutylideneacetic acid
CAS:<p>2-Cyclobutylideneacetic acid</p>Formula:C6H8O2Purity:97%Color and Shape: white solidMolecular weight:112.13g/mol2-Cyclobutylideneacetic acid
CAS:<p>2-Cyclobutylideneacetic acid is a monomer that inhibits protein synthesis by binding to the amino acids in the polypeptide chain. It also has been shown to be an inhibitor of epidermal growth factor and linker, which are proteins involved in angiogenesis. 2-Cyclobutylideneacetic acid has been shown to have cardiovascular benefits due to its ability to inhibit cholesterol ester transfer. This drug also exhibits tautomerism, which may account for the stereoisomers observed in the laboratory.</p>Formula:C6H8O2Purity:Min. 95%Molecular weight:112.13 g/mol



