Ordering
Available Variants1 g
CHA.22098-1g
Price
€28.00
Available – Dispatch in 14 days
5 g
CHA.22098-5g
Price
€52.08
Available – Dispatch in 14 days
25 g
CHA.22098-25g
Price
€87.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.22098-1g | €28.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.22098-5g | €52.08 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.22098-25g | €87.20 |
≥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 | FC6H4B(OH)2 |
|---|---|
| CAS Number | 1765-93-1 |
| Molecular Weight | 139.92 |
| UNSPSC Code | 12352103 |
| NACRES | NA.22 |
| PubChem Substance ID | 24866160 |
| MDL number | MFCD00039136 |
| Beilstein/REAXYS Number | 2829653 |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302,H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 4 Oral - 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
4-Fluorophenylboronic acid, with the CAS number 1765-93-1, is a boronic acid derivative that has gained significant attention in various fields of organic chemistry. This compound is widely used as a building block in the synthesis of complex molecules, including pharmaceuticals and materials. The presence of the fluorine atom on the phenyl ring imparts unique properties to the molecule, such as increased reactivity and stability. 4-Fluorophenylboronic acid is commonly employed in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds with high efficiency and selectivity. Its applications extend to the development of new drugs, agrochemicals, and functional materials, highlighting the importance of this versatile compound in modern chemistry. The compounds properties and reactivity make it a valuable tool for researchers and chemists in various industries.
