Ordering
Available Variants500 mg
CHA.24642-500mg
Price
€71.40
Available – Dispatch in 14 days
2 g
CHA.24642-2g
Price
€154.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.24642-500mg | €71.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
2 g | CHA.24642-2g | €154.80 |
≥95.0%
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
| Empirical Formula (Hill Notation) | C4H9BO2 |
|---|---|
| CAS Number | 849052-26-2 |
| Molecular Weight | 99.92 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883473 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD06798108 |
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
Cyclobutylboronic acid, with the CAS registry number 849052-26-2, is a boronic acid derivative that has garnered significant attention in the realm of organic synthesis. This compound is characterized by its unique cyclobutyl moiety, which is attached to a boronic acid functional group, thereby rendering it a valuable intermediate in various chemical reactions. The versatility of cyclobutylboronic acid stems from its ability to participate in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of complex molecules with high precision. Furthermore, its relatively small ring size imparts distinct steric and electronic properties, making it an attractive building block for the synthesis of pharmaceuticals, agrochemicals, and materials science applications. As a result, cyclobutylboronic acid has become a sought-after reagent in modern organic chemistry, facilitating the creation of novel compounds with potential applications in diverse fields.
