Description
(4-Propylphenyl)boronic acid (CAS No. 134150-01-9) is a high-purity boronic acid derivative with the molecular formula C9H13BO2. This organoboron compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its excellent reactivity and stability. The compound features a propylphenyl group attached to a boronic acid moiety, making it a valuable building block for pharmaceuticals, agrochemicals, and advanced materials. Our product is rigorously tested to ensure ≥95% purity (HPLC) and is supplied as a white to off-white crystalline powder. Suitable for research and industrial applications, it is packaged under inert conditions to guarantee long-term stability.
Key Specifications:
• CAS Number: 134150-01-9
• Molecular Weight: 164.01 g/mol
• Purity: ≥95% (HPLC)
• Appearance: White to off-white powder
• Storage: Store at 2-8°C under inert atmosphere
Properties
- CAS Number: 134150-01-9
- Complexity: 120
- IUPAC Name: (4-propylphenyl)boronic acid
- InChI: InChI=1S/C9H13BO2/c1-2-3-8-4-6-9(7-5-8)10(11)12/h4-7,11-12H,2-3H2,1H3
- InChI Key: WLCGYIWOKVWFLB-UHFFFAOYSA-N
- Exact Mass: 164.1008598
- Molecular Formula: C9H13BO2
- Molecular Weight: 164.01
- SMILES: B(C1=CC=C(C=C1)CCC)(O)O
- Topological: 40.5
- Monoisotopic Mass: 164.1008598
- Synonyms: (4-propylphenyl)boronic Acid, 4-Propylphenylboronic acid, 134150-01-9, 4-(Propyl)benzeneboronic acid, 4-propylbenzeneboronic acid, MFCD00859261, CHEMBL1952295, 4-Propylphenylboronicacid, 4-Propylphenyl boronic acid, Boronic acid, (4-propylphenyl)-, 4-N-PROPYLPHENYLBORONIC ACID, 4-propyl phenylboronic acid, p-n-propylphenyl boronic acid, SCHEMBL257735, 4-n-propyl-phenyl boronic acid, DTXSID00399320, BCP22762, BDBM50364282, SBB071049, AKOS004116362, AB07462, BCP9000144, CS-W016096, DS-0669, HY-W015380, AC-24817, BP-11441, SY021200, DB-005359, EN300-117472, Z336079950
Application
(4-Propylphenyl)boronic acid is a versatile reagent in palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura couplings, to form biaryl structures prevalent in drug discovery. It serves as a key intermediate in synthesizing liquid crystals and organic electronic materials. Researchers also employ it in proteomics and bioconjugation studies due to its selective binding with diols and other functional groups.
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