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Available Variants1 g
CHA.38763-1g
Price
€65.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.38763-1g | €65.40 |
95%
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) | C11H15BFNO2 |
|---|---|
| CAS Number | 458532-88-2 |
| Molecular Weight | 223.05 |
| NACRES | NA.22 |
| PubChem Substance ID | 329762463 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD06798251 |
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 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
3-Fluoro-4-pyridineboronic acid pinacol ester, with the CAS number 458532-88-2, is a versatile intermediate in organic synthesis. This compound is a boronic ester, which is a class of molecules that have been widely used in various chemical reactions, including Suzuki-Miyaura cross-coupling reactions. The presence of the fluoro substituent on the pyridine ring imparts unique electronic properties to the molecule, making it a valuable building block for the synthesis of complex molecules. The pinacol ester moiety provides a stable and easily removable protecting group, allowing for further functionalization of the boronic acid. This compound has been employed in the synthesis of a range of molecules, including pharmaceuticals and materials, and its applications continue to expand as new synthetic methodologies are developed. Its properties make it a valuable tool in modern organic synthesis.
