CAS 30830-28-5

3-(1,1-Dimethylethoxy)cyclobutanone

Description:

3-(1,1-Dimethylethoxy)cyclobutanone is an organic compound characterized by its cyclobutanone structure, which features a four-membered carbon ring with a ketone functional group. The presence of the 1,1-dimethylethoxy group introduces steric hindrance and influences the compound's reactivity and physical properties. This substance is typically a colorless to pale yellow liquid, exhibiting a distinctive odor. It is soluble in organic solvents, which is common for many ketones, but its solubility in water is limited due to its hydrophobic nature. The compound may participate in various chemical reactions, including nucleophilic additions and rearrangements, owing to the reactive carbonyl group. Its unique structure and properties make it of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken due to potential hazards associated with its use.

Formula: C₈H₁₄O₂

InChI: InChI=1S/C8H14O2/c1-8(2,3)10-7-4-6(9)5-7/h7H,4-5H2,1-3H3

InChI key: InChIKey=URYFBVQQZFUJSM-UHFFFAOYSA-N

SMILES: O(C(C)(C)C)C1CC(=O)C1

Synonyms:

• Cyclobutanone, 3-(1,1-dimethylethoxy)-
• Cyclobutanone, 3-tert-butoxy-
• 3-(1,1-Dimethylethoxy)cyclobutanone
• 3-[(1,1-Dimethylethyl)oxy]cyclobutanone

3-(tert-butoxy)cyclobutan-1-one

CAS: 30830-28-5

Formula: C₈H₁₄O₂

Purity: 98%

Molecular weight: 142.1956

Ref: IN-DA01A5BS

3-(tert-Butoxy)cyclobutan-1-one

CAS: 30830-28-5

3-(tert-Butoxy)cyclobutan-1-one

Molecular weight: 142.19556g/mol

Ref: 54-OR1021377

-3(tert-butoxy)cyclobutanone

CAS: 30830-28-5

The compound (-3(tert-butoxy)cyclobutanone) is a stereoselective hydroxylation of 4-cyanopyridine catalyzed by acetonitrile in the presence of sodium as a base. The reaction product is an unsymmetrical aldehyde with two hydroxyl groups on opposite sides of the ring. This synthesis can be carried out in one step, and the amines that are used as starting materials can be varied to synthesize different products. The reaction proceeds via nucleophilic attack on the nitro group of 5-nitroquinoline by chloride ion to yield an intermediate that undergoes hydrolysis with water and elimination of chloride ion to give 2-hydroxy-5-(tosyloxy)pyridine. This intermediate then reacts with ferrocene and vinyl ether in acetonitrile to give (-3(tert-butoxy)cyclobutanone).

Formula: C₈H₁₄O₂

Purity: Min. 95%

Molecular weight: 142.2 g/mol

Ref: 3D-FBA83028