Ordering
Available Variants1 g
CHA.73756-1g
Price
€95.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.73756-1g | €95.40 |
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
| Empirical Formula (Hill Notation) | C13H16BFO4 |
|---|---|
| CAS Number | 1050423-87-4 |
| Molecular Weight | 266.07 |
| NACRES | NA.22 |
| PubChem Substance ID | 329763756 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD12756466 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
4-Carboxy-2-fluorophenylboronic acid pinacol ester, with the CAS number 1050423-87-4, is a boronic acid ester that has gained significant attention in the field of organic synthesis. This compound is a versatile building block used in various chemical reactions, including Suzuki-Miyaura cross-coupling reactions, which enable the formation of complex molecules. The presence of the fluorine atom and the carboxylic acid functional group in the molecule provides a unique combination of properties, making it an attractive intermediate for the synthesis of pharmaceuticals, agrochemicals, and materials. The pinacol ester moiety protects the boronic acid functionality, allowing for easier handling and storage, and can be readily cleaved under basic conditions to reveal the boronic acid, which can then participate in further reactions. This compound is widely used in research and development applications.
