Description

1-Bromocyclobutanecarboxylic acid (CAS No. 32122-23-9) is a high-purity brominated cyclobutane derivative with the molecular formula C₅H₇BrO₂. This compound is a versatile building block in organic synthesis, particularly for the preparation of cyclobutane-containing scaffolds. Its IUPAC name is 1-bromocyclobutane-1-carboxylic acid, and it is characterized by a cyclobutane ring substituted with a bromine atom and a carboxylic acid group at the same carbon. This reagent is ideal for researchers working on pharmaceuticals, agrochemicals, and material science applications where cyclobutane rings are desired. Available in various quantities, our product is rigorously tested for purity and stability to ensure optimal performance in your experiments.

Properties

• CAS Number: 32122-23-9
• Complexity: 118
• IUPAC Name: 1-bromocyclobutanecarboxylic acid
• InChI: InChI=1S/C5H7BrO2/c6-5(4(7)8)2-1-3-5/h1-3H2,(H,7,8)
• InChI Key: YREQYUFYDFSXJC-UHFFFAOYSA-N
• Exact Mass: 177.96294
• Molecular Formula: C5H7BrO2
• Molecular Weight: 179.01
• SMILES: C1CC(C1)(C(=O)O)Br
• Topological: 37.3
• Monoisotopic Mass: 177.96294
• Synonyms: 1-Bromocyclobutanecarboxylic acid, 32122-23-9, 1-bromocyclobutane-1-carboxylic acid, DTXSID10306727, DTXCID40257854, 837-467-2, MFCD08861855, Cyclobutanecarboxylic acid, 1-bromo-, NSC179441, 3GC3JAU3L9, 1-Bromocyclobutanecarboxylicacid, SCHEMBL1159185, YREQYUFYDFSXJC-UHFFFAOYSA-N, HBA12223, CL4587, AKOS022172452, NSC 179441, NSC-179441, AS-45982, SY129843, DB-068586, CS-0040826, EN300-102949, Z220564362

Application

1-Bromocyclobutanecarboxylic acid is widely used as a key intermediate in the synthesis of cyclobutane-based compounds, which are valuable in medicinal chemistry for drug discovery. It serves as a precursor for the preparation of cyclobutane-containing analogs of bioactive molecules, enabling structure-activity relationship (SAR) studies. Additionally, this compound is employed in materials science for the development of novel polymers and functionalized materials. Its reactivity in nucleophilic substitution and coupling reactions makes it a versatile tool for synthetic chemists.

Safety and Hazards

GHS Hazard Statements

• H302 (66.7%): Harmful if swallowed [Warning Acute toxicity, oral]
• H314 (66.7%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
• H315 (33.3%): Causes skin irritation [Warning Skin corrosion/irritation]
• H318 (66.7%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
• H335 (33.3%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P362+P364, P363, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (66.7%)
• Skin Corr. 1B (66.7%)
• Skin Irrit. 2 (33.3%)
• Eye Dam. 1 (66.7%)
• STOT SE 3 (33.3%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.