4-Iodophenylboronic acid pinacol ester
4-Iodophenylboronic acid pinacol ester (CAS: 73852-88-7, C12H16BIO2) is a versatile organoboron compound with a molecular weight of 329.97. This aryl boronate ester serves as a key building block in organic synthesis, particularly in cross-coupling reactions. Its utility spans the development of pharmaceuticals, agrochemicals, and advanced materials, making it an indispensable reagent for researchers and industrial chemists.
- IUPAC
- 2-(4-Iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- Synonyms
- 2-(4-Iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Suzuki-Miyaura Cross-Coupling Reactions
As a boronate ester, it readily participates in palladium-catalyzed Suzuki-Miyaura couplings. This reaction is fundamental for forming carbon-carbon bonds, enabling the synthesis of complex biaryl structures prevalent in drug discovery and materials science.
Organic Synthesis Reagent
This compound is a valuable intermediate for introducing the 4-iodophenyl moiety into various organic frameworks. It is employed in multi-step syntheses requiring precise functional group manipulation and carbon skeleton construction.
Pharmaceutical Intermediate
Its structure is incorporated into numerous biologically active molecules. It facilitates the development of novel therapeutic agents by providing a reactive handle for molecular elaboration in pharmaceutical research.
Materials Science
The compound can be utilised in the synthesis of organic electronic materials, such as those used in OLEDs or organic semiconductors, where specific aryl frameworks are required for desired electronic properties.
| Molecular weight | 329.97 |
|---|---|
| Empirical formula | C12H16BIO2 |
| Assay | 97% |
| Melting point | 101-105 °C |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is 4-Iodophenylboronic acid pinacol ester used for?
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4-Iodophenylboronic acid pinacol ester is primarily used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for forming carbon-carbon bonds. It is a valuable intermediate in the development of pharmaceuticals, agrochemicals, and advanced materials.
What are the CAS number and formula for 4-Iodophenylboronic acid pinacol ester?
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The CAS number is 73852-88-7 and the empirical formula is C12H16BIO2.
What grade and purity does Tech Serve Solutions supply?
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Tech Serve Solutions supplies 4-Iodophenylboronic acid pinacol ester with an assay of 97%. This product is suitable for research and chemical synthesis applications. It is not represented as USP, BP, EP, or other pharmacopoeia grades.
What are the safety precautions for handling 4-Iodophenylboronic acid pinacol ester?
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Handling requires appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter should be used. Consult the Safety Data Sheet (SDS) for comprehensive handling information and hazard details.
How is 4-Iodophenylboronic acid pinacol ester packed, shipped, and exported?
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Products are carefully packed to ensure integrity during transit. Tech Serve Solutions is experienced in exporting chemicals globally, adhering to all relevant shipping regulations. Specific packaging details can be provided upon request.
How can I request a sample or a quote for 4-Iodophenylboronic acid pinacol ester?
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To request a sample or a quotation, please contact our sales department via the website or by phone, specifying the product name and CAS number.
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