trans-2-Phenylvinylboronic acid MIDA ester
Tech Serve Solutions offers trans-2-Phenylvinylboronic acid MIDA ester (CAS: 1152427-93-4, Formula: C13H14BNO4) with a molecular weight of 259.07 g/mol. This organometallic reagent is a key building block in organic synthesis. It is specifically utilised in Suzuki cross-coupling reactions, facilitated by its MIDA boronate structure, enabling the efficient formation of carbon-carbon bonds in complex molecule construction. Available at 95% purity.
Suzuki Cross-Coupling Reactions
This compound is an effective reagent for Suzuki-Miyaura cross-coupling reactions. The MIDA ester functionality offers stability and controlled reactivity, making it ideal for synthesising biaryl compounds and other complex organic structures.
Organic Synthesis Building Block
As a functionalised boronate ester, it serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its structure allows for precise incorporation into various molecular frameworks.
MIDA Boronate Chemistry
It exemplifies the utility of MIDA boronates in modern synthetic chemistry. These reagents are known for their stability towards chromatography and ease of handling compared to traditional boronic acids.
| Molecular weight | 259.07 |
|---|---|
| Empirical formula | C13H14BNO4 |
| Assay | 95% |
| Application | Suzuki Cross-Coupling with MIDA Boronates |
| Melting point | 185-195 °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 trans-2-Phenylvinylboronic acid MIDA ester used for?
+
trans-2-Phenylvinylboronic acid MIDA ester is primarily used as a reagent in Suzuki cross-coupling reactions for the synthesis of complex organic molecules.
What is the CAS number and formula for trans-2-Phenylvinylboronic acid MIDA ester?
+
The CAS number is 1152427-93-4 and the molecular formula is C13H14BNO4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies trans-2-Phenylvinylboronic acid MIDA ester with an assay of 95%. We do not represent this product as USP, BP, or EP grade.
What are the safety and handling considerations for this chemical?
+
This compound requires the use of eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. Refer to the Safety Data Sheet for comprehensive handling information.
How is trans-2-Phenylvinylboronic acid MIDA ester packed, shipped, and exported?
+
Tech Serve Solutions ensures appropriate packaging for safe transport and handles global export procedures for this chemical.
How can I request a sample or quote for trans-2-Phenylvinylboronic acid MIDA ester?
+
Please contact our sales team via the website or by calling our dedicated line to request a sample or a formal quotation.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis