CAS 113681-11-1

Cyclopentanone,3-(hydroxymethyl)-, (3S)-

Description:

Cyclopentanone, 3-(hydroxymethyl)-, (3S)-, with the CAS number 113681-11-1, is a chiral organic compound characterized by a cyclopentanone ring with a hydroxymethyl group attached at the 3-position. This compound features a five-membered cyclic ketone structure, which contributes to its unique chemical properties, including its reactivity and potential for forming hydrogen bonds due to the presence of the hydroxymethyl group. The (3S) designation indicates the specific stereochemistry of the molecule, which can influence its biological activity and interactions with other substances. Cyclopentanone derivatives are often studied for their applications in organic synthesis and as intermediates in the production of pharmaceuticals and agrochemicals. The presence of the hydroxymethyl group can enhance solubility in polar solvents and may also affect the compound's volatility and boiling point. Overall, this compound is of interest in both synthetic organic chemistry and medicinal chemistry due to its structural features and potential applications.

Formula: C₆H₁₀O₂

Synonyms:

• Cyclopentanone,3-(hydroxymethyl)-, (S)-

Cyclopentanone, 3-(hydroxymethyl)-, (3S)-

CAS: 113681-11-1

Formula: C₆H₁₀O₂

Purity: 97%

Molecular weight: 114.1424

Ref: IN-DA00099Z

3-(hydroxymethyl)cyclopentanone

CAS: 113681-11-1

3-Hydroxymethylcyclopentanone is a precursor to synthesize methyl epijasmonate.

Formula: C₆H₁₀O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 114.14

Ref: TM-TN2951

3-(Hydroxymethyl)cyclopentanone

CAS: 113681-11-1

Formula: C₆H₁₀O₂

Purity: 95%~99%

Color and Shape: Oil

Molecular weight: 114.144

Ref: BP-SBP00686

3-(Hydroxymethyl)cyclopentanone

Controlled Product

CAS: 113681-11-1

Formula: C₆H₁₀O₂

Color and Shape: Neat

Molecular weight: 114.142

Ref: TR-H283950

3-(Hydroxymethyl)cyclopentanone

CAS: 113681-11-1

3-(Hydroxymethyl)cyclopentanone is a bifunctional molecule that can be used as a catalyst. It is able to catalyze the hydration of ketones and esters, which is an important reaction for the synthesis of carbocyclic nucleosides. 3-(Hydroxymethyl)cyclopentanone has been shown to react with dilithium (LiH), forming a covalent bond through its two functional groups. The long-chain nature of this molecule makes it ideal for use in hydrophobic environments such as those found in tumor cells. 3-(Hydroxymethyl)cyclopentanone also exhibits dichroism, which is caused by the different absorption of light when passing through a crystalline substance. This property can be utilized to study the stereoisomeric structure of molecules with similar chemical properties such as 5-hydroxymethylfurfural (HMF).

Formula: C₆H₁₀O₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 114.14 g/mol

Ref: 3D-FH15931