Cas no 1030832-38-2 (5-Fluoro-2-methylphenylboronic Acid Pinacol Ester)
5-Fluoro-2-methylphenylboronic Acid Pinacol Ester Chemical and Physical Properties
Names and Identifiers
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- 5-Fluoro-2-methylphenylboronic acid pinacol ester
- 5-Fluoro-2-Methylbenzeneboronic acid pinacol ester, 97%
- 2-(5-Fluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- MFCD18729893
- 3-fluoro-6-methylphenylboronic acid pinacol ester
- 1030832-38-2
- 5-Fluoro-2-Methylbenzeneboronic acid pinacol ester
- EN300-202253
- AKOS017550056
- BS-26112
- AT16182
- DB-391670
- CS-0174942
- ZTKSYTPCVNDCIE-UHFFFAOYSA-N
- 5-Fluoro-2-methylphenylboronic Acid Pinacol Ester
-
- MDL: MFCD18729893
- Inchi: 1S/C13H18BFO2/c1-9-6-7-10(15)8-11(9)14-16-12(2,3)13(4,5)17-14/h6-8H,1-5H3
- InChI Key: ZTKSYTPCVNDCIE-UHFFFAOYSA-N
- SMILES: FC1C=CC(C)=C(B2OC(C)(C)C(C)(C)O2)C=1
Computed Properties
- Exact Mass: 236.1383881g/mol
- Monoisotopic Mass: 236.1383881g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 17
- Rotatable Bond Count: 1
- Complexity: 277
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 18.5?2
5-Fluoro-2-methylphenylboronic Acid Pinacol Ester Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM204392-1g |
2-(5-Fluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
1030832-38-2 | 95% | 1g |
$59 | 2021-08-04 | |
| Chemenu | CM204392-5g |
2-(5-Fluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
1030832-38-2 | 95% | 5g |
$218 | 2021-08-04 | |
| Chemenu | CM204392-25g |
2-(5-Fluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
1030832-38-2 | 95% | 25g |
$792 | 2021-08-04 | |
| TRC | F596538-100mg |
5-Fluoro-2-methylphenylboronic Acid Pinacol Ester |
1030832-38-2 | 100mg |
$64.00 | 2023-05-18 | ||
| TRC | F596538-250mg |
5-Fluoro-2-methylphenylboronic Acid Pinacol Ester |
1030832-38-2 | 250mg |
$75.00 | 2023-05-18 | ||
| TRC | F596538-500mg |
5-Fluoro-2-methylphenylboronic Acid Pinacol Ester |
1030832-38-2 | 500mg |
$87.00 | 2023-05-18 | ||
| TRC | F596538-1g |
5-Fluoro-2-methylphenylboronic Acid Pinacol Ester |
1030832-38-2 | 1g |
$98.00 | 2023-05-18 | ||
| Chemenu | CM204392-1g |
2-(5-Fluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
1030832-38-2 | 95% | 1g |
$59 | 2022-06-14 | |
| Chemenu | CM204392-5g |
2-(5-Fluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
1030832-38-2 | 95% | 5g |
$323 | 2023-02-03 | |
| Chemenu | CM204392-25g |
2-(5-Fluoro-2-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
1030832-38-2 | 95% | 25g |
$792 | 2022-06-14 |
5-Fluoro-2-methylphenylboronic Acid Pinacol Ester Related Literature
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Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
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2. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
Additional information on 5-Fluoro-2-methylphenylboronic Acid Pinacol Ester
Recent Advances in the Application of 5-Fluoro-2-methylphenylboronic Acid Pinacol Ester (CAS: 1030832-38-2) in Chemical Biology and Pharmaceutical Research
The compound 5-Fluoro-2-methylphenylboronic Acid Pinacol Ester (CAS: 1030832-38-2) has garnered significant attention in recent years due to its versatile applications in chemical biology and pharmaceutical research. As a boronic acid derivative, this compound plays a crucial role in Suzuki-Miyaura cross-coupling reactions, which are pivotal for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Recent studies have highlighted its potential in drug discovery, particularly in the development of kinase inhibitors and other targeted therapies.
One of the most notable advancements involving 5-Fluoro-2-methylphenylboronic Acid Pinacol Ester is its use in the synthesis of novel tyrosine kinase inhibitors. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its efficacy as a key intermediate in the production of compounds targeting EGFR (Epidermal Growth Factor Receptor) mutations, which are implicated in various cancers. The study reported that the boronic ester moiety facilitated efficient coupling reactions, leading to high yields and purity of the final products. This underscores the compound's importance in streamlining the synthesis of potential anticancer agents.
In addition to its role in drug synthesis, 5-Fluoro-2-methylphenylboronic Acid Pinacol Ester has been explored for its utility in proteolysis-targeting chimeras (PROTACs). A recent preprint on bioRxiv detailed its incorporation into bifunctional molecules designed to degrade specific disease-causing proteins. The boronic acid group's ability to form reversible covalent bonds with target proteins makes it an attractive candidate for PROTAC development, offering a promising avenue for tackling previously undruggable targets.
Further research has also investigated the compound's physicochemical properties, such as its stability and reactivity under various conditions. A 2022 paper in Organic Process Research & Development highlighted the optimization of reaction conditions for large-scale synthesis, addressing challenges related to hydrolysis and byproduct formation. These findings are critical for industrial applications, ensuring the compound's reliable production for pharmaceutical manufacturing.
Looking ahead, the potential of 5-Fluoro-2-methylphenylboronic Acid Pinacol Ester extends beyond its current applications. Ongoing studies are exploring its use in bioconjugation techniques and as a probe for studying enzyme mechanisms. With its unique chemical properties and versatility, this compound is poised to remain a cornerstone in chemical biology and drug discovery research. Future directions may include its integration into more complex molecular architectures and its application in emerging therapeutic modalities such as covalent inhibitors and targeted protein degradation.
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