Description
(4-Fluoro-5-isopropyl-2-methoxyphenyl)boronic acid (CAS No. 875446-29-0) is a high-purity boronic acid derivative with the molecular formula C10H14BFO3. This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its reactive boronic acid functional group. The presence of fluoro, isopropyl, and methoxy substituents on the phenyl ring enhances its utility in the synthesis of complex pharmaceutical intermediates and agrochemicals. Our product is rigorously tested for purity (>95% by HPLC) and is supplied as a white to off-white crystalline powder, ensuring consistent performance in your research applications. Store in a cool, dry place under inert conditions to maintain stability.
Properties
- CAS Number: 875446-29-0
- Complexity: 201
- IUPAC Name: (4-fluoro-5-isopropyl-2-methoxy-phenyl)boronic acid
- InChI: InChI=1S/C10H14BFO3/c1-6(2)7-4-8(11(13)14)10(15-3)5-9(7)12/h4-6,13-14H,1-3H3
- InChI Key: HMRRCUXJGOSJJA-UHFFFAOYSA-N
- Exact Mass: 212.1020026
- Molecular Formula: C10H14BFO3
- Molecular Weight: 212.03
- SMILES: B(C1=CC(=C(C=C1OC)F)C(C)C)(O)O
- Topological: 49.7
- Monoisotopic Mass: 212.1020026
- Synonyms: (4-Fluoro-5-isopropyl-2-methoxyphenyl)boronic acid, 810-448-6, 875446-29-0, 4-fluoro-5-isopropyl-2-methoxyphenylboronic acid, [4-fluoro-2-methoxy-5-(propan-2-yl)phenyl]boronic acid, (4-fluoro-2-methoxy-5-propan-2-ylphenyl)boronic acid, MFCD16294183, Boronic acid, [4-fluoro-2-methoxy-5-(1-methylethyl)phenyl]-, SCHEMBL135122, DTXSID90693642, HMRRCUXJGOSJJA-UHFFFAOYSA-N, BCP12755, CS-M3091, AKOS016005659, GS-6333, AC-27373, SY012631, DB-077004, F1024, (4-Fluoro-5-isopropyl-2-methoxyphenyl)boronicacid, (4-Fluoro-5-isopropyl-2-methoxy-phenyl)boronic acid, 4-Fluoro-5-isopropyl-2-methoxyphenylboronic Acid (contains varying amounts of Anhydride)
Application
This boronic acid derivative is widely used in pharmaceutical research for the synthesis of bioactive molecules and drug candidates. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions to form biaryl structures, which are prevalent in many therapeutic agents. Additionally, its unique substitution pattern makes it suitable for developing agrochemicals and functional materials.
Safety and Hazards
GHS Hazard Statements
- H302 (50%): Harmful if swallowed [Warning Acute toxicity, oral]
- H315 (50%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (50%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
Precautionary Statements
- P264, P264+P265, P270, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (50%)
- Eye Irrit. 2 (50%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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