ChemicalBook > Product Catalog >Chemical Reagents >Organic reagents >Boric acid >4-Formylphenylboronic acid
4-Formylphenylboronic acid
![4-Formylphenylboronic acid Structure](CAS/GIF/87199-17-5.gif)
- CAS No.
- 87199-17-5
- Chemical Name:
- 4-Formylphenylboronic acid
- Synonyms
- FPBA;4-FORMYLBENZENEBORONIC ACID;AKOS BRN-0111;TIMTEC-BB SBB004077;RARECHEM AH PB 0193;4-Formylphenylboroni;4-Formylboronic acid;4-BORONOBENZALDEHYDE;Metoprolol Impurity 34;4-Formylpenylboronic Acid
- CBNumber:
- CB1491072
- Molecular Formula:
- C7H7BO3
- Molecular Weight:
- 149.94
- MOL File:
- 87199-17-5.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/4/28 15:15:04
Melting point | 237-242 °C (lit.) |
---|---|
Boiling point | 347.6±44.0 °C(Predicted) |
Density | 1.24±0.1 g/cm3(Predicted) |
vapor pressure | 0Pa at 25℃ |
storage temp. | Keep in dark place,Sealed in dry,Room Temperature |
solubility | <10g/l |
form | Liquid |
pka | 7.34±0.10(Predicted) |
color | Clear colorless to yellow-orange |
PH | 5.5 (1g/l, H2O, 20℃) |
Water Solubility | Slightly Soluble in water. |
Sensitive | Air Sensitive |
BRN | 3030770 |
InChIKey | VXWBQOJISHAKKM-UHFFFAOYSA-N |
LogP | 1.36 at 20℃ |
CAS DataBase Reference | 87199-17-5(CAS DataBase Reference) |
EPA Substance Registry System | Boronic acid, (4-formylphenyl)- (87199-17-5) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | ![]() GHS07 |
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Signal word | Warning | |||||||||
Hazard statements | H317 | |||||||||
Precautionary statements | P261-P272-P280-P302+P352-P333+P313-P362+P364 | |||||||||
Hazard Codes | C,Xi | |||||||||
Risk Statements | 34-36/37/38 | |||||||||
Safety Statements | 22-26-36/37/39-45-37/39-36 | |||||||||
RIDADR | UN 1759 8/PG 3 | |||||||||
WGK Germany | 3 | |||||||||
F | 10 | |||||||||
Hazard Note | Irritant | |||||||||
TSCA | T | |||||||||
HazardClass | IRRITANT, AIR SENSITIVE | |||||||||
HS Code | 29163990 | |||||||||
NFPA 704 |
|
4-Formylphenylboronic acid price More Price(10)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich(India) | 431966 | 4-Formylphenylboronic acid ≥95.0% | 87199-17-5 | 1G | ₹2170 | 2022-06-14 | Buy |
Sigma-Aldrich(India) | 431966 | 4-Formylphenylboronic acid ≥95.0% | 87199-17-5 | 5G | ₹7761.53 | 2022-06-14 | Buy |
Sigma-Aldrich(India) | 431966 | 4-Formylphenylboronic acid ≥95.0% | 87199-17-5 | 25G | ₹18930 | 2022-06-14 | Buy |
ALFA India | ALF-B25199-14 | 4-Formylbenzeneboronic acid, 97% | 87199-17-5 | 25g | ₹28791 | 2022-05-26 | Buy |
ALFA India | ALF-B25199-06 | 4-Formylbenzeneboronic acid, 97% | 87199-17-5 | 5g | ₹6209 | 2022-05-26 | Buy |
4-Formylphenylboronic acid Chemical Properties,Uses,Production
Chemical Properties
white to light yellow crystal powder
Uses
4-Formylphenylboronic acid is a substrate for Suzuki cross-coupling reactions and it can be used as a reagent for:
- Palladium-catalyzed 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.
- The synthesis of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells.
- The synthesis of a novel protein synthesis inhibitor active against Gram-positive bacteria.
- The Suzuki aryl-aryl coupling of the upper rim of hexahomotrioxacalix[3]arene.
- A rhodium-catalyzed cyclization, converting 1,5-enynes to cyclopentenes and spiro-cyclopentenes.
Synthesis
Potassium phenyltrifluoroborate (184 mg, 1.00 mmol) was added to a solution of iron trichloride (185 mg, 1.10 mmol) in 3 mL of 1:1 THF/water. The mixture was stirred at room temperature for 30 min. The reaction mixture was then passed through a short column containing neutral absorption alumina. The alumina was then washed with a mixture of ethyl acetate/hexanes (2:1) to obtain 4-Formylphenylboronic acid (105 mg, 86%). [The boronic acid products can also be isolated by simple extraction techniques.]
4-Formylphenylboronic acid Preparation Products And Raw materials
Raw materials
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1,3,5-Tris(p-formylphenyl)benzene
(2-(4-vinylphenyl)ethene-1,1,2-triyl)tribenzene
3,4'-DIHYDROXYFLAVONE
4-(2-Cyanophenyl)benzaldehyde
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Global( 529)Suppliers
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TRC FINE CHEMS | +91-7400278327 +91-8097105248 | Mumbai, India | 73 | 58 | Inquiry |
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87199-17-5(4-Formylphenylboronic acid)Related Search:
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RARECHEM AH PB 0193
TIMTEC-BB SBB004077
P-FORMYLPHENYLBORONIC ACID
AKOS BRN-0111
4-FORMYLPHENYLBORONIC ACID
4-BORONOBENZALDEHYDE
4-(Dihydroxyboryl)benzaldehyde, 4-Boronobenzaldehyde
4-Formylboronic acid
4-Formylphenylboronic acid ,97%
4-Formylphenylboronic acid,4-(Dihydroxyboryl)benzaldehyde, 4-Boronobenzaldehyde
4-Formylphenylboroni
4-ForMylphenylboronic acid, 97% 1GR
Benzeneboronic acid, p-forMyl- (6CI,7CI)
4-ForMylphenylboronic acid >=95.0%
4-Formylphenylboronic acid
4-(Dihydroxyboryl)benzaldehyde
p-Formylbenzeneboronic acid
(4-methanoylphenyl)boronic acid
Boronic acid, (4-formylphenyl)-
4-(dihydroxyboryl)benzaldehyde
BENZALDEHYDE-4-BORONIC ACID
4-Boronobenzaldehyde~4-Formylphenylboronic acid
4-Formylpenylboronic Acid
Boronic acid, (4-formylphenyl)- (9CI)
4-Formylbenzeneboronicacid,97%
4-Formylphenylboronic acid(FPBA)
2,4-DINITROTOLUENE,1X1ML, ACN 1000UG/ML
PARAFORMYLPHENYLBORONIC ACID
4-FORMYLPHENYLBORONIC ACID, 98+%
4-Formylphenlboronic acid
4-Formylphenylboronic Acid (contains varying amounts of Anhydride)
Boronic acid, B-(4-formylphenyl)-
4-Formylphenylboronic Acid extrapure, 95%
4-FORMYLBENZENEBORONIC ACID
FPBA
4-Formylphenylboronic acid (4-FPBA)
Metoprolol Impurity 34
87199-17-5
87199-17-2
Boronic Acids
B (Classes of Boron Compounds)
BORONIC ACID
Boronic Acids and Derivatives
Aryl
Organometallic Reagents
Substituted Boronic Acids
Boron, Nitrile, Thio,& TM-Cpds
Carbonyl Compounds
ALDEHYDE
Aldehydes
blocks
BoronicAcids
Boronic Acid series
Aryl
Organoborons
B (Classes of Boron Compounds)
CHIRAL CHEMICALS
Boronic Acids & Esters
Boronic Acid