CHA.35044
4-Amino-3-fluorophenylboronic acid hydrochloride
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Ordering
Available Variants1 g
CHA.35044-1g
Price
€187.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.35044-1g | €187.20 |
Professionally catalogued chemical listing prepared to support identification, technical review, safety visibility, and structured B2B sourcing workflows.
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
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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) | C6H8BClFNO2 |
|---|---|
| CAS Number | 1256355-32-4 |
| Molecular Weight | 191.40 |
| NACRES | NA.22 |
| PubChem Substance ID | 329763645 |
| UNSPSC Code | 12352103 |
| MDL number | MFCD11867880 |
Safety Information Handling visibility
| pictograms |
GHS07
GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302 |
| Hazard Classifications | Acute Tox. 4 Oral |
| 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-Amino-3-fluorophenylboronic acid hydrochloride, with a CAS number of 494752-42-0, is a chemical compound that has garnered significant attention in the realm of organic synthesis and medicinal chemistry. This boronic acid derivative is commonly utilized as a building block in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. The presence of the amino and fluorine substituents on the phenyl ring imparts unique properties to the molecule, making it a valuable intermediate in various cross-coupling reactions. The hydrochloride salt form of the compound enhances its stability and solubility, facilitating its handling and use in a range of chemical transformations. As a result, 4-amino-3-fluorophenylboronic acid hydrochloride has become a staple in many synthetic chemistry laboratories, enabling the efficient construction of complex molecules with diverse applications.
