| Identification | More | [Name]
DIBENZOFURAN-4-BORONIC ACID | [CAS]
100124-06-9 | [Synonyms]
4-DIBENZOFURANBORONIC ACID
AKOS BRN-0085
DIBENZO[B,D]FURAN-4-YLBORONIC ACID
DIBENZOFURAN-4-BORONIC ACID
RARECHEM AH PB 0052
TIMTEC-BB SBB003426
Dibenzofuran-4-boronic acid, 98+%
dibenzofuran-4-ylboronic acid
4-(Dibenzofuranyl)boronic acid | [EINECS(EC#)]
672-293-9 | [Molecular Formula]
C12H9BO3 | [MDL Number]
MFCD00092336 | [Molecular Weight]
212.01 | [MOL File]
100124-06-9.mol |
| Chemical Properties | Back Directory | [Appearance]
off-white to beige powder | [Melting point ]
286-291 °C (lit.) | [Boiling point ]
438.5±37.0 °C(Predicted) | [density ]
1.34±0.1 g/cm3(Predicted) | [storage temp. ]
0-6°C | [form ]
powder | [pka]
8.04±0.30(Predicted) | [color ]
white to off-white | [BRN ]
1645426 | [InChIKey]
ZXHUJRZYLRVVNP-UHFFFAOYSA-N | [CAS DataBase Reference]
100124-06-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [TSCA ]
No | [HazardClass ]
IRRITANT | [HS Code ]
29321900 |
| Hazard Information | Back Directory | [Description]
Dibenzofuran-4-boronic acid (DBFBA) is a boronic acid that has been used
as a cross-coupling agent in the Suzuki coupling reaction. It has been
shown to have low efficiency, but advances in this area have been made
through the use of methanol extraction and photophysical properties.
DBFBA is often coupled with imidazole derivatives to form
anti-inflammatory compounds. The bond cleavage and hydrogen bonding
properties of DBFBA make it a good target for drug synthesis.
| [Chemical Properties]
off-white to beige powder | [Synthesis]
In a 300 ml three-necked flask, 7.2 g of 4-bromodibenzofuran was dissolved in -78° C. anhydrous tetrahydrofuran (THF) under an argon atmosphere. Then, 20 ml of an n-butyl lithium-n-hexane solution (1.6 M, 1.1 eq) was added and stirred for 1 hour. 4.23 ml (1.3 eq) of trimethoxyborane (B(OMe)3) was added and stirred for 2 hours, and the temperature of the reaction system was increased to room temperature. 200 ml of 1 N hydrochloric acid was added into the reactant and stirred for 3 hours. An organic layer was separated, and solvents were distilled off. In the crude product thus obtained, hexane was added. Precipitated product was filtered to obtain 4.94 g of dibenzofuran-4-boronic acid as a white solid (yield 80%). |
|
|