Description

Cyclobutanecarbaldehyde (CAS No. 2987-17-9) is a high-purity organic compound with the molecular formula C₅H₈O, widely utilized in synthetic chemistry and pharmaceutical research. This aldehyde derivative of cyclobutane features a reactive carbonyl group, making it a valuable intermediate for the synthesis of heterocyclic compounds, fragrances, and specialty chemicals. Our product is rigorously tested to ensure superior quality, with consistent purity levels suitable for demanding laboratory and industrial applications. Available in various quantities, Cyclobutanecarbaldehyde is supplied in tightly sealed containers to maintain stability and prevent degradation. Researchers and chemists rely on this compound for its versatility in organic transformations, including Grignard reactions, reductive amination, and cycloaddition processes.

Properties

• CAS Number: 2987-17-9
• Complexity: 55
• IUPAC Name: cyclobutanecarbaldehyde
• InChI: InChI=1S/C5H8O/c6-4-5-2-1-3-5/h4-5H,1-3H2
• InChI Key: INVYSLWXPIEDIQ-UHFFFAOYSA-N
• Exact Mass: 84.057514874
• Molecular Formula: C5H8O
• Molecular Weight: 84.12
• SMILES: C1CC(C1)C=O
• Topological: 17.1
• Monoisotopic Mass: 84.057514874
• Synonyms: Cyclobutanecarboxaldehyde, cyclobutanecarbaldehyde, 2987-17-9, DTXSID70498011, CYCLOBUTANE CARBALDEHYDE, DTXCID40448821, 608-426-4, MFCD03789631, CHEMBL18475, Cyclobutanaldehyde; Cyclobutylcarboxaldehyde; Formylcyclobutane, cyclobutancarbaldehyd, cyclobutanecarboaldehyde, 2-cyclobutanecarbaldehyde, cyclobutane carboxaldehyde, SCHEMBL37813, SCHEMBL37814, SCHEMBL9032325, SCHEMBL9032363, SCHEMBL16445367, SCHEMBL27511905, INVYSLWXPIEDIQ-UHFFFAOYSA-N, BCP28808, CS-D0314, BBL100220, BDBM50028845, cyclobutanecarboxaldehyde, AldrichCPR, STL553793, AKOS012298721, SB85395, PS-11985, SY019700, EN300-71825, Z1079442452

Application

Cyclobutanecarbaldehyde serves as a key building block in organic synthesis, particularly in the preparation of cyclobutane-containing pharmaceuticals and agrochemicals. It is employed in the development of flavor and fragrance compounds due to its unique structural properties. Researchers also utilize this aldehyde in metal-catalyzed coupling reactions and as a precursor for chiral ligand synthesis.

Safety and Hazards

GHS Hazard Statements

• H302 (90.9%): Harmful if swallowed [Warning Acute toxicity, oral]
• H319 (95.5%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

• P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P330, P337+P317, and P501

Hazard Classes and Categories

• Acute Tox. 4 (90.9%)
• Eye Irrit. 2A (95.5%)

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