Ordering
Available Variants5 g
CHA.52316-5g
Price
€22.16
Available – Dispatch in 14 days
25 g
CHA.52316-25g
Price
€46.88
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.52316-5g | €22.16 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.52316-25g | €46.88 |
≥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.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | (CH3O)2C6H3B(OH)2 |
|---|---|
| CAS Number | 23112-96-1 |
| Molecular Weight | 181.98 |
| NACRES | NA.22 |
| PubChem Substance ID | 24871546 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD01318987 |
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
2,6-Dimethoxyphenylboronic acid, with the CAS registry number 23112-96-1, is a boronic acid derivative that has garnered significant attention in the realm of organic synthesis. This compound is widely utilized as a building block in the construction of complex molecules, particularly in the context of Suzuki-Miyaura cross-coupling reactions. The presence of the dimethoxy substituents on the phenyl ring imparts unique electronic and steric properties to the molecule, rendering it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials. Furthermore, 2,6-dimethoxyphenylboronic acid has been employed in the development of novel catalytic systems and has shown promise in the formation of carbon-carbon and carbon-heteroatom bonds, thereby underscoring its importance in modern organic chemistry. Its applications continue to expand, driven by ongoing research and advancements in the field.
