| Identification | More | [Name]
2-Chloropyridine-5-boronic acid | [CAS]
444120-91-6 | [Synonyms]
2-CHLORO-5-PYRIDINEBORONIC ACID
2-CHLORO-5-PYRIDYL BORONIC ACID
2-CHLOROPYRIDIN-5-YLBORONIC ACID
2-CHLOROPYRIDINE-5-BORONIC ACID
6-CHLORO-3-PYRIDINEBORONIC ACID
6-CHLORO-3-PYRIDINYLBORONIC ACID
6-CHLOROPYRIDIN-3-YL-3-BORONIC ACID
(6-CHLOROPYRIDIN-3-YL)BORONIC ACID
6-CHLOROPYRIDINE-3-BORONIC ACID
AKOS BRN-0199
RARECHEM AK ML 0442
2-Chlorpyridine-5-boronic acid
Boronic acid, (6-chloro-3-pyridinyl)-(9CI)
2-Chloropyridine-5-Boronic
6-chloro-3-pyridylboronic acid
2-Chloro-5-pyridineboronic Acid (contains varying amounts of Anhydride)
2-Chloropyridine-5-boronic acid ,96%
Boronic acid, B-(6-chloro-3-pyridinyl)- | [EINECS(EC#)]
628-524-0 | [Molecular Formula]
C5H5BClNO2 | [MDL Number]
MFCD03094998 | [Molecular Weight]
157.36 | [MOL File]
444120-91-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
165 °C(lit.) | [Boiling point ]
336.9±52.0 °C(Predicted) | [density ]
1.41±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [pka]
6.70±0.10(Predicted) | [Detection Methods]
HPLC,NMR | [BRN ]
9119810 | [InChIKey]
WPAPNCXMYWRTTL-UHFFFAOYSA-N | [CAS DataBase Reference]
444120-91-6(CAS DataBase Reference) |
| 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 .
S36/37:Wear suitable protective clothing and gloves . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29333990 |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white solid | [Uses]
6-Chloro-3-pyridinylboronic acid can be used:
- To prepare biologically significant 3-arylcoumarins by reacting with 3-chlorocoumarin through Suzuki reaction.
- As a substrate in the synthesis of 11-(pyridinylphenyl)steroid with progesterone agonist/antagonist profile.
- As a substrate in the preparation of α- secondary and tertiary pyridines by the reaction of pyridotriazoles with boronic acids.
- As a substrate in the palladium-catalyzed α-arylation of saturated cyclic amines and N-methyl amines.
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