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4-Formylbenzeneboronic acid, 97%

CAS: 87199-17-5 | C7H7BO3 | 149.94 g/mol

Supplier:  Thermo Scientific Chemicals B2519914

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Catalog No. AAB2519914


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Description

Description

4-Formylbenzeneboronic acid acts as a reagent used for Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids, triethylamine-catalyzed three-component Hantzsch condensations, copper-catalyzed nitrations, oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta, palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides, palladium-catalyzed aerobic oxidative cross-coupling reactions. It acts as a reagent used in preparation of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells, a novel protein synthesis inhibitor active against Gram-positive bacteria.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Formylbenzeneboronic acid acts as a reagent used for Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids, triethylamine-catalyzed three-component Hantzsch condensations, copper-catalyzed nitrations, oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta, palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides, palladium-catalyzed aerobic oxidative cross-coupling reactions. It acts as a reagent used in preparation of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells, a novel protein synthesis inhibitor active against Gram-positive bacteria.

Solubility
Slightly Soluble in water.

Notes
Air Sensitive. Store away from air and oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Specifications

Specifications

4-Formylbenzeneboronic acid
260°C to 266°C
MFCD00151823
3030770
4-formylphenyl boronic acid, 4-formylbenzeneboronic acid, 4-boronobenzaldehyde, boronic acid, 4-formylphenyl, boronic acid, b-4-formylphenyl, p-formylphenylboronic acid, 4-dihydroxyboryl benzaldehyde, 4-dihydroxyboranyl benzaldehyde, 4-benzaldehyde boronic acid, 4-formyl-phenylboronic acid
VXWBQOJISHAKKM-UHFFFAOYSA-N
(4-formylphenyl)boronic acid
591073
97%
87199-17-5
C7H7BO3
25 g
Air Sensitive
Slightly Soluble in water.
OB(O)C1=CC=C(C=O)C=C1
149.94
149.94

Chemical Identifiers

87199-17-5
149.94
VXWBQOJISHAKKM-UHFFFAOYSA-N
591073
OB(O)C1=CC=C(C=O)C=C1
C7H7BO3
MFCD00151823
4-formylphenyl boronic acid, 4-formylbenzeneboronic acid, 4-boronobenzaldehyde, boronic acid, 4-formylphenyl, boronic acid, b-4-formylphenyl, p-formylphenylboronic acid, 4-dihydroxyboryl benzaldehyde, 4-dihydroxyboranyl benzaldehyde, 4-benzaldehyde boronic acid, 4-formyl-phenylboronic acid
(4-formylphenyl)boronic acid
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Safety and Handling

Safety and Handling

GHS H Statement
H317
May cause an allergic skin reaction.

P261-P272-P280g-P302+P352-P333+P313-P363-P501c

H317

EINECSNumber : 438-670-5

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
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