4-Formylphenylboronic acid

• Catalog No.: 431966
• CAS Number: 87199-17-5
• M. F.: C7H7BO3
• M. W.: 149.93968
• Purity: ≥95.0%

SYNONYMS

• Title: 4-甲酰基苯硼酸
• IUPAC name: (4-formylphenyl)boronic acid
• IUPAC Traditional name: 4-formylphenylboronic acid
• Synonyms: 4-Boronobenzaldehyde; 4-(Dihydroxyboryl)benzaldehyde; 对甲酰苯硼酸; 4-Formylbenzeneboronic acid; p-Formylbenzeneboronic acid; p-Formylphenylboronic acid; 4-醛基苯硼酸

DATABASE IDS

• PubChem SID: 24867058
• Beilstein Number: 3030770
• CAS Number: 87199-17-5
• MDL Number: MFCD00151823

PROPERTIES

• GHS Signal Word: Danger
• GHS Hazard statements: H314-H317
• European Hazard Symbols: Corrosive (C)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
• GHS Precautionary statements: P280-P305 + P351 + P338-P310
• RID/ADR: UN 1759 8/PG 3
• Risk Statements: 34
• Safety Statements: 22-26-36/37/39-45
• Hazard Class: 8
• UN Number: 1759
• Packing Group: 3
• German water hazard class: 3
• Linear Formula: HCOC6H4B(OH)2
• Purity: ≥95.0%
• Melting Point: 237-242 °C(lit.)

DETAILS

Description (简体中文)

Other Notes
含不定量的酸酐
包装
1, 5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water1
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2
• Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids3
• Triethylamine-catalyzed three-component Hantzsch condensations4
• Copper-catalyzed nitrations5
• Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta6
• Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides7
• Palladium-catalyzed aerobic oxidative cross-coupling reactions8 Reagent used in Preparation of
• Sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells9
• A novel protein synthesis inhibitor active against Gram-positive bacteria10

Description (English)

Other Notes
Contains varying amounts of anhydride
Packaging
1, 5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water1
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2
• Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids3
• Triethylamine-catalyzed three-component Hantzsch condensations4
• Copper-catalyzed nitrations5
• Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta6
• Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides7
• Palladium-catalyzed aerobic oxidative cross-coupling reactions8 Reagent used in Preparation of
• Sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells9
• A novel protein synthesis inhibitor active against Gram-positive bacteria10