| Identification | More | [Name]
2-Chloro-3-pyridylboronic acid | [CAS]
381248-04-0 | [Synonyms]
2-CHLORO-3-PYRIDINEBORONIC ACID
2-CHLORO-3-PYRIDINYL-BORONIC ACID
2-CHLORO-3-PYRIDYL BORONIC ACID
2-CHLOROPYRIDIN-3-YLBORONIC ACID
2-CHLOROPYRIDINE-3-BORONIC ACID
AKOS BRN-0504
3-Chlorpyridine-3-boronic acid
2-Chloro-5-Trimethoxyphenylboronic acid
Boronic acid, (2-chloro-3-pyridinyl)-(9CI)
2-Chloropyridine-3-Boronic
2-Chloro-3-pyridilboronic acid
2-CHLORO-3-PYRIDIEBORONICACID
2-Chloropyridine-3-boronic acid 96%
Boronic acid, B-(2-chloro-3-pyridinyl)- | [EINECS(EC#)]
624-435-6 | [Molecular Formula]
C5H5BClNO2 | [MDL Number]
MFCD03094997 | [Molecular Weight]
157.36 | [MOL File]
381248-04-0.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
2811 | [WGK Germany ]
3 | [Hazard Note ]
Irritant/Keep Cold | [HazardClass ]
IRRITANT | [HS Code ]
29333990 |
| Hazard Information | Back Directory | [Chemical Properties]
White solid | [Uses]
Reactant for:
- Synthesis of Et canthinone-3-carboxylates from Et 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate via a Pd-catalyzed Suzuki-Miyaura coupling and a Cu-catalyzed amidation reaction
- Preparation of arylmethylpyrrolidinylmethanols and amine derivatives via reaction with MIDA followed by Suzuki reaction with halides or amination with amines
- Preparation of arylazabicyclooctane derivatives as potential arginine vasopressin receptor antagonists
- Regioselective preparation of halo-oligopyridines and oligopyridines by the Suzuki-Miyaura cross-coupling reaction
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