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Available Variants5 g
CHA.92023-5g
Price
€87.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.92023-5g | €87.20 |
97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
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Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C18H28B2O4 |
|---|---|
| CAS Number | 99770-93-1 |
| Molecular Weight | 330.03 |
| NACRES | NA.22 |
| PubChem Substance ID | 24884661 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD08276852 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
1,4-Benzenediboronic acid bis(pinacol) ester, with the CAS number 99770-93-1, is a versatile organoboron compound that has gained significant attention in the field of organic synthesis. This compound is widely used as a building block in the construction of complex molecules, particularly in the context of cross-coupling reactions. The pinacol ester moiety serves as a protective group, stabilizing the boronic acid functionality and facilitating its handling and storage. The 1,4-benzenediboronic acid bis(pinacol) ester is commonly employed in Suzuki-Miyaura coupling reactions, allowing for the formation of carbon-carbon bonds between aryl halides and other organoboron compounds. Its high reactivity and selectivity make it a valuable tool in the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and materials science applications.
