CAS 20614-90-8

Cyclobutanone, 3-(1,1-dimethylethyl)-

Description:

Cyclobutanone, 3-(1,1-dimethylethyl)-, also known by its CAS number 20614-90-8, is a cyclic ketone characterized by a four-membered cyclobutane ring with a ketone functional group and a tert-butyl substituent at the 3-position. This compound typically exhibits a colorless to pale yellow liquid form and has a distinctive odor. Its molecular structure contributes to its unique chemical properties, including moderate volatility and solubility in organic solvents. Cyclobutanone derivatives are of interest in organic synthesis and can serve as intermediates in the production of various pharmaceuticals and agrochemicals. The presence of the tert-butyl group enhances its steric hindrance, which can influence reactivity and stability. Additionally, cyclobutanones may participate in various chemical reactions, such as nucleophilic additions and rearrangements, making them valuable in synthetic organic chemistry. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested.

Formula: C₈H₁₄O

Cyclobutanone, 3-(1,1-dimethylethyl)-

CAS: 20614-90-8

Formula: C₈H₁₄O

Purity: 97%

Color and Shape: Liquid

Molecular weight: 126.1962

Ref: IN-DA00IL6K

3-tert-Butylcyclobutanone

CAS: 20614-90-8

3-tert-Butylcyclobutanone

Purity: ≥95%

Molecular weight: 126.20g/mol

Ref: 54-OR304353

3-tert-Butylcyclobutanone

CAS: 20614-90-8

Purity: 98%

Molecular weight: 126.1989975

Ref: 10-F609461

3-tert-butylcyclobutan-1-one

Controlled Product

CAS: 20614-90-8

Formula: C₈H₁₄O

Color and Shape: Neat

Molecular weight: 126.196

Ref: TR-B871965

3-tert-Butylcyclobutanone

CAS: 20614-90-8

3-tert-Butylcyclobutanone is an organocatalyst that is used for the asymmetric synthesis of cyclobutanones. It has been shown to be a chiral, stereoselective and catalytic mediator in the Baeyer–Villiger oxidation of enones. 3-tert-Butylcyclobutanone also exhibits self-assembly properties and can form dimers with other molecules. This compound is also capable of catalyzing cycloadditions between electron deficient alkenes and electron rich dienes. The dimers of 3-tert-butylcyclobutanone are formed by hydrogen bonding interactions between the keto groups on adjacent molecules.

Formula: C₈H₁₄O

Purity: Min. 95%

Molecular weight: 126.2 g/mol

Ref: 3D-VAA61490