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4-(DIHYDROXYBORYL)PHENYLBORONIC ACID

1,4-Benzenediboronic acid

CAS: 4612-26-4

Molecular Formula: C6H8B2O4

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4-(DIHYDROXYBORYL)PHENYLBORONIC ACID - Names and Identifiers

Name 1,4-Benzenediboronic acid
Synonyms AKOS BRN-0002
1,4-Phenyldiboronic acid
P-PHENYLENEDIBORONIC ACID
1,4-Benzenediboronic acid
1,4-BENZENEDIBORONIC ACID
Benzene-1,4-diboronic acid
BENZENE-1,4-DIBORONIC ACID
1,4-PHENYLENEDIBORONIC ACID
1,4-Phenylenediboronic acid
1,4-Phenylenebisboronic acid
benzene-1,4-diyldiboronic acid
1,4-PHENYLENEBIS(BORONIC ACID)
4-(Dihydroxyboryl)phenylboronic acid
4-(DIHYDROXYBORYL)PHENYLBORONIC ACID
CAS 4612-26-4
EINECS 628-888-0
InChI InChI=1/C6H8B2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4,9-12H
InChIKey BODYVHJTUHHINQ-UHFFFAOYSA-N

4-(DIHYDROXYBORYL)PHENYLBORONIC ACID - Physico-chemical Properties

Molecular FormulaC6H8B2O4
Molar Mass165.75
Density1.33±0.1 g/cm3(Predicted)
Melting Point>350°C(lit.)
Boling Point420.1±55.0 °C(Predicted)
Flash Point207.9°C
Water SolubilitySoluble in water 2.5%.
Solubility soluble in Methanol
Vapor Presure8.27E-08mmHg at 25°C
AppearanceSolid
Colorwhite to off-white
BRN2836921
pKa8.30±0.17(Predicted)
Storage ConditionKeep in dark place,Sealed in dry,Room Temperature
Refractive Index1.555
MDLMFCD00236018
UseReagent used for . Externally initiated Kumada catalyst-transfer polycondensation . Suzuki-Miyaura cross-coupling reactions . Energy transfer processes in optoelectronic devices . Palladium-catalyzed sequential alkenylation and conjugate addition rea

4-(DIHYDROXYBORYL)PHENYLBORONIC ACID - Risk and Safety

Risk CodesR22 - Harmful if swallowed
R36/37/38 - Irritating to eyes, respiratory system and skin.
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety DescriptionS36 - Wear suitable protective clothing.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3
TSCANo
HS Code29310095
Hazard NoteCorrosive
Hazard ClassIRRITANT

4-(DIHYDROXYBORYL)PHENYLBORONIC ACID - Reference Information

use p-phenyldiboronic acid can be used as an intermediate in pharmaceutical synthesis.
preparation compound m(8.87g,37.6mmol) is dissolved in tetrahydrofuran (140mL), hexane solvent and 2.5M n-butyl lithium (18mL,45.1mmol) are added dropwise at -78 ℃, and then stirred for 1 hour. After slowly adding trimethyl borate (13mL,56.4mmol), stir for 2 hours. Then add 2M hydrochloric acid to neutralize, and extract the product with ethyl acetate and water. Recrystallization with dichloromethane and hexane to obtain the compound p-phenyldiboronic acid n(2.93g,47%).
Last Update:2024-04-10 22:29:15
4-(DIHYDROXYBORYL)PHENYLBORONIC ACID
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View History
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