Identification | More | [Name]
3-Formylphenylboronic acid | [CAS]
87199-16-4 | [Synonyms]
3-BORONOBENZALDEHYDE 3-(DIHYDROXYBORYL)BENZALDEHYDE 3-FORMYLBENZENEBORONIC ACID 3-FORMYLBORONIC ACID 3-FORMYLPHENYLBORONIC ACID AKOS BRN-0110 AURORA 15117 BENZALDEHYDE-3-BORONIC ACID IFLAB-BB F1371-0205 M-FORMYLPHENYLBORONIC ACID OTAVA-BB BB7110951391 RARECHEM AH PB 0194 TIMTEC-BB SBB004078 ZERENEX ZX001648 3-Boronobenzaldehyde~3-Formylphenylboronic acid 3-Formylpenylboronic Acid Boronic acid, (3-formylphenyl)-(9CI) 3-FORMYLPHENYLBORONIC ACID (CONTAINS VARYING AMOUNTS OF ANHYDRIDE) 3-(Dihydroxyboryl)benzaldehyde, 3-Boronobenzaldehyde | [EINECS(EC#)]
628-589-5 | [Molecular Formula]
C7H7BO3 | [MDL Number]
MFCD00161356 | [Molecular Weight]
149.94 | [MOL File]
87199-16-4.mol |
Chemical Properties | Back Directory | [Appearance]
Off-white Cryst | [Melting point ]
109-113 °C | [Boiling point ]
354.4±44.0 °C(Predicted) | [density ]
1.24±0.1 g/cm3(Predicted) | [storage temp. ]
0-6°C | [solubility ]
soluble in Methanol | [form ]
Powder, Crystals, and/or Chunks | [pka]
7.83±0.10(Predicted) | [color ]
Off-white to beige or light orange | [Sensitive ]
Air Sensitive | [BRN ]
3030769 | [InChI]
InChI=1S/C7H7BO3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-5,10-11H | [InChIKey]
HJBGZJMKTOMQRR-UHFFFAOYSA-N | [SMILES]
B(C1=CC=CC(C=O)=C1)(O)O | [CAS DataBase Reference]
87199-16-4(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R34:Causes burns. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S22:Do not breathe dust . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S37/39:Wear suitable gloves and eye/face protection . S27:Take off immediately all contaminated clothing . | [RIDADR ]
UN 3261 8/PG 3
| [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT, MOISTURE SENSITIVE | [PackingGroup ]
Ⅲ | [HS Code ]
29319099 |
Raw materials And Preparation Products | Back Directory | [Raw materials]
Magnesium, bromo[3-(dimethoxymethyl)phenyl]--->Boroxin, 2,4,6-tris(3-bromophenyl)--->3-Tolylboronic acid-->N,N-Dimethylformamide-->Trimethyl borate-->Sulfuric acid-->Tetrahydrofuran | [Preparation Products]
(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol-->3-(4-METHYLPHENYL)BENZALDEHYDE-->3-(1,3-THIAZOL-2-YL)BENZALDEHYDE-->3-benzylbenzaldehyde-->2'-Nitro-biphenyl-3-carbaldehyde-->3-(6-Methoxynaphthalen-2-yl)benzaldehyde-->Benzaldehyde, 3-(benzoyloxy)-
-->3-PHENYLETHYNYL-BENZALDEHYDE |
Hazard Information | Back Directory | [Chemical Properties]
Off-white Cryst | [Uses]
Reagent used:
- To study the effects of boronic acid on fluoride-selective chemosignaling behavior of merocyanine dye
- As exciton-coupled CD probes for epigallocatechin gallate
Biological inhibitor of γ-glutamyltranspeptidase
Reactant involved in:
- Palladium-catalyzed homocoupling
- Suzuki coupling reactions
| [Uses]
3-Formylphenylboronic acid can be used as reagent to study the effects of boronic acid on fluoride-selective chemosignaling behavior of merocyanine dye and as exciton-coupled CD probes for epigallocatechin gallate Biological inhibitor of γ-glutamyltranspeptidase.
| [Uses]
suzuki reaction | [Synthesis]
The general procedure for the synthesis of 3-formylphenylboronic acid from the compound (CAS:540777-53-5) and trimethyl borate was carried out as follows: firstly, a THF solution of trimethyl borate was prepared by adding 154.8 ml of trimethyl borate to a 3-liter three-necked flask, followed by 915 ml of tetrahydrofuran (THF). The solution was stirred under nitrogen protection and cooled with an ice bath. The cooled THF solution was slowly added to a 3-liter flask containing Grignard reagent through a stainless steel tube. The reaction mixture was stirred under ice bath cooling for 1 hour and then an aqueous sulfuric acid solution prepared from 30 ml of concentrated sulfuric acid and 480 ml of water was added. The temperature of the mixture was gradually brought to room temperature and stirring was continued at this temperature for 2 hours. After stopping stirring, the reaction mixture was allowed to stand at room temperature overnight. The precipitate was removed by filtration and the filtrate was concentrated. The concentrated residue was mixed with an equal volume of water and stirred at room temperature for 1 hour. The solid product was collected by filtration and dried to give 123.46 g of 3-formylphenylboronic acid in 88% yield. The 1H-NMR (200 MHz, CDCl3, δ ppm) data of the resulting product were as follows: 7.54 (t, J = 7.5 Hz, 1H), 7.93 (d, J = 6.1 Hz, 1H), 7.9-8.1 (br.d, 1H), 8.2-8.3 (br.s, 1H), 10.04 (s, 1H). | [References]
[1] BARTOSZ ZARYCHTA. 3-formylphenylboronic acid.[J]. Acta crystallographica. Section C, Crystal structure communications, 2004, 60 Pt 5: o344-5. DOI:10.1107/S0108270104006493. [2] E. TANI?. Conformational, Structural, Vibrational, Electronic, and Molecular Docking Studies of 3-Formylphenylboronic Acid and 4-Formylphenylboronic Acid: A Comparative Study[J]. Russian Journal of Physical Chemistry A, 2020, 94 13: 2784-2796. DOI:10.1134/S0036024420130282. |
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