Ordering
Available Variants25 g
CHA.18196-25g
Price
€228.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.18196-25g | €228.00 |
≥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
| Linear Formula | F2C6H3B(OH)2 |
|---|---|
| CAS Number | 156545-07-2 |
| Molecular Weight | 157.91 |
| NACRES | NA.22 |
| PubChem Substance ID | 24870772 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD01318138 |
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 |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
3,5-Difluorophenylboronic acid, with the CAS number 156545-07-2, is a boronic acid derivative that has garnered significant attention in the realm of organic synthesis and medicinal chemistry. This compound is particularly useful as a building block in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. The presence of two fluorine atoms on the phenyl ring imparts unique electronic properties, making it an attractive intermediate for the preparation of fluorinated compounds. The boronic acid functional group allows for facile participation in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds with various aryl and heteroaryl partners. As a result, 3,5-difluorophenylboronic acid has become a valuable tool in the synthesis of biologically active molecules and materials with potential applications in various fields. Its versatility and reactivity make it a sought-after reagent in modern organic synthesis.
