3-Aminophenylboronic acid hydrochloride
ALDRICH/410705 - 98%
Synonym: (m-Aminophenyl)boronic acid hydrochloride; 3-
CAS Number: 85006-23-1
Empirical Formula (Hill Notation): C6H8BNO2 · HCl
Molecular Weight: 173.41
EC Number: 285-052-4
MDL Number: MFCD00191748
Linear Formula: H2NC6H4B(OH)2 · HCl
Product Type: Chemical
| assay | 98% |
| form | powder |
| InChI | 1S/C6H8BNO2.ClH/c8-6-3-1- |
| InChI key | QBMHZZHJIBUPOX-UHFFFAOYSA |
| SMILES string | Cl.Nc1cccc(c1)B(O)O |
| Application: | 3-Aminophenylboronic acid hydrochloride was used as a key reagent used in the synthesis of the boronic acid ester starting material, which is subsequently converted to the cyclobutene precursor through a Heck coupling reaction. It is also used as a boronic acid source in the synthesis of boronate-functionalized monomers. These monomers are further used in the preparation of reproducible and high-quality polymer films. |
| General description: | 3-Aminophenylboronic acid hydrochloride is a boronic acid derivative that is commonly used as a reagent in Suzuki-Miyaura coupling reactions, where it can be used to form C-C bonds by the reaction with aryl or vinyl halides. It can also be used in other cross-coupling reactions, such as copper-catalyzed coupling reactions, as well as in palladium-free cross-coupling reactions. |
| Packaging: | 1, 5 g in glass bottle |
| Symbol |  GHS07 |
| Signal word | Warning |
| Hazard statements | H315 - H319 - H335 |
| Precautionary statements | P302 + P352 - P305 + P351 + P338 |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 98% |
| UNSPSC | 12352103 |