| Identification | More | [Name]
3,5-Dichlorophenylboronic acid | [CAS]
67492-50-6 | [Synonyms]
3,5-DICHLOROBENZENEBORONIC ACID
3,5-DICHLOROPHENYLBORONIC ACID
AKOS BRN-0088
RARECHEM AH PB 0088
3,5-Dichlophenylboronic acid
3,5-Dichlorobenzeneboronicacid,98%
3,5-DICHLOROPHENYLBORONIC ACID 98%
3,5-Dichlorophenylboronic 97% +
3,5-Dichlorophenylboronic Acid (contains varying amounts of Anhydride)
3,5-Dichlorophenylboronic acid ,98% | [Molecular Formula]
C6H5BCl2O2 | [MDL Number]
MFCD00051935 | [Molecular Weight]
190.82 | [MOL File]
67492-50-6.mol |
| Chemical Properties | Back Directory | [Appearance]
white to off-white powder | [Melting point ]
315 °C | [Boiling point ]
351.7±52.0 °C(Predicted) | [density ]
1.47±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
powder to crystal | [pka]
6.58±0.10(Predicted) | [color ]
White to Almost white | [BRN ]
7581091 | [CAS DataBase Reference]
67492-50-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn,F | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R22:Harmful if swallowed.
R19:May form explosive peroxides.
R11:Highly Flammable. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection .
S33:Take precautionary measures against static discharges .
S16:Keep away from sources of ignition-No smoking . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29319099 |
| Hazard Information | Back Directory | [Chemical Properties]
white to off-white powder | [Uses]
3,5-Dichlorobenzeneboronic Acid, is an intermediate for the synthesis of various pharmaceutical compounds including inhibitors. 3,5-Dichlorobenzeneboronic Acid was also found to facilitate the transport of various ribonucleosides in and out of liposomes (artificial cells). | [Uses]
Reactant involved in:• ;Suzuki-Miyaura cross-coupling1,2• ;Trifluoromethylation3• ;Intramolecular aromatic carbenoid insertion of biaryldiazoacetates4• ;Cyanation for the synthesis of aromatic nitriles5• ;Lithiation of dihalophenyl dioxazaborocines for synthesis of functionalized dihalophenyl boronic acid6 | [Uses]
suzuki reaction |
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