CAS 27610-27-1

Solerole

Description:

Solerole, with the CAS number 27610-27-1, is a chemical compound that belongs to the class of organic compounds known as alcohols. It is characterized by the presence of a hydroxyl (-OH) functional group, which imparts certain properties typical of alcohols, such as solubility in water and the ability to participate in hydrogen bonding. Solerole is often utilized in various industrial applications, including as a solvent or in the synthesis of other chemical compounds. Its molecular structure contributes to its reactivity and interaction with other substances. Additionally, like many organic compounds, Solerole may exhibit specific physical properties such as boiling and melting points, density, and viscosity, which are influenced by its molecular weight and structure. Safety data sheets should be consulted for handling and storage guidelines, as well as potential health effects associated with exposure. Overall, Solerole is a versatile compound with applications in both research and industry.

Formula: C₆H₁₀O₃

InChI: InChI=1S/C6H10O3/c1-4(7)5-2-3-6(8)9-5/h4-5,7H,2-3H2,1H3

InChI key: InChIKey=KBLZKAKKJPDYKJ-UHFFFAOYSA-N

SMILES: C(C)(O)C1OC(=O)CC1

Synonyms:

• 2(3H)-Furanone, dihydro-5-(1-hydroxyethyl)-
• 27610-27-1
• 4,5-Dihydroxyhexanoic acid γ-lactone
• Dihydro-5-(1-hydroxyethyl)-2(3H)-furanone
• Solerole

Solerole

Controlled Product

CAS: 27610-27-1

Applications Solerole is derived from 2-Iodoacetamide (I685505), which is an alkylating agent commonly used in the alkylation of proteins.
References Woods, A.G.,et. al.: Biochem. Bioph. Res. Co., 419, 305 (2012); Samgina, T.Y., et. al.: J. Am. Soc. Mass Spec., 22, 2246 (2011)

Formula: C₆H₁₀O₃

Color and Shape: Neat

Molecular weight: 130.14

Ref: TR-S676630

5-(1-Hydroxyethyl)oxolan-2-one

CAS: 27610-27-1

5-(1-Hydroxyethyl)oxolan-2-one (5-HEOL) is a chiral compound. It is a potential new drug for the treatment of fungal infections. 5-HEOL has been shown to inhibit growth in vitro, and it also shows good efficacy in an animal model that mimics human infection with Candida albicans. This compound has been found to be safe and effective when administered orally to mice. The effect of 5-HEOL is stereoselective; it inhibits the growth of C. albicans yeast cells by blocking fatty acid synthesis at the level of transcription, while not affecting the production of fatty acids by mammalian cells.

Formula: C₆H₁₀O₃

Purity: Min. 95%

Molecular weight: 130.14 g/mol

Ref: 3D-CBA61027