Cas no 1056955-09-9 (butyl 2-fluoro-6-hydroxybenzoate)
butyl 2-fluoro-6-hydroxybenzoate Chemical and Physical Properties
Names and Identifiers
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- Butyl 2-Fluoro-6-hydroxybenzoate
- Benzoic acid, 2-fluoro-6-hydroxy-, butyl ester
- butyl 2-fluoro-6-hydroxybenzoate
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- Inchi: 1S/C11H13FO3/c1-2-3-7-15-11(14)10-8(12)5-4-6-9(10)13/h4-6,13H,2-3,7H2,1H3
- InChI Key: KNOCDDFZXSUPCH-UHFFFAOYSA-N
- SMILES: C(OCCCC)(=O)C1=C(O)C=CC=C1F
butyl 2-fluoro-6-hydroxybenzoate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B812270-50mg |
Butyl 2-Fluoro-6-hydroxybenzoate |
1056955-09-9 | 50mg |
$ 70.00 | 2022-06-06 | ||
| TRC | B812270-100mg |
Butyl 2-Fluoro-6-hydroxybenzoate |
1056955-09-9 | 100mg |
$ 95.00 | 2022-06-06 | ||
| TRC | B812270-500mg |
Butyl 2-Fluoro-6-hydroxybenzoate |
1056955-09-9 | 500mg |
$ 365.00 | 2022-06-06 | ||
| Enamine | EN300-192644-0.05g |
butyl 2-fluoro-6-hydroxybenzoate |
1056955-09-9 | 95% | 0.05g |
$53.0 | 2023-09-17 | |
| Enamine | EN300-192644-0.1g |
butyl 2-fluoro-6-hydroxybenzoate |
1056955-09-9 | 95% | 0.1g |
$83.0 | 2023-09-17 | |
| Enamine | EN300-192644-0.25g |
butyl 2-fluoro-6-hydroxybenzoate |
1056955-09-9 | 95% | 0.25g |
$116.0 | 2023-09-17 | |
| Enamine | EN300-192644-0.5g |
butyl 2-fluoro-6-hydroxybenzoate |
1056955-09-9 | 95% | 0.5g |
$218.0 | 2023-09-17 | |
| Enamine | EN300-192644-1g |
butyl 2-fluoro-6-hydroxybenzoate |
1056955-09-9 | 95% | 1g |
$314.0 | 2023-09-17 | |
| Enamine | EN300-192644-2.5g |
butyl 2-fluoro-6-hydroxybenzoate |
1056955-09-9 | 95% | 2.5g |
$614.0 | 2023-09-17 | |
| Enamine | EN300-192644-5g |
butyl 2-fluoro-6-hydroxybenzoate |
1056955-09-9 | 95% | 5g |
$908.0 | 2023-09-17 |
butyl 2-fluoro-6-hydroxybenzoate Related Literature
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
Additional information on butyl 2-fluoro-6-hydroxybenzoate
Comprehensive Guide to Butyl 2-Fluoro-6-Hydroxybenzoate (CAS No. 1056955-09-9): Properties, Applications, and Market Insights
Butyl 2-fluoro-6-hydroxybenzoate (CAS No. 1056955-09-9) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This ester derivative, featuring a fluoro and hydroxy functional group on the aromatic ring, exhibits unique chemical properties that make it valuable for synthetic applications. With the growing demand for fluorinated compounds in drug discovery, this molecule is increasingly studied for its potential in creating bioactive intermediates.
The compound's molecular structure combines a butyl ester group with a fluorinated benzoate core, offering both lipophilicity and electronic effects that are critical in modern organic synthesis. Researchers are particularly interested in its role as a building block for pharmaceutical intermediates, where the fluoro substituent can significantly alter biological activity. Recent studies highlight its utility in developing anti-inflammatory agents and antimicrobial compounds, aligning with current healthcare trends focusing on novel therapeutic approaches.
From a chemical perspective, butyl 2-fluoro-6-hydroxybenzoate demonstrates interesting solubility characteristics, being moderately soluble in organic solvents while showing limited water solubility. This property profile makes it particularly useful in organic synthesis applications where controlled reactivity is desired. The presence of both electron-withdrawing (fluoro) and electron-donating (hydroxy) groups creates a unique electronic environment that synthetic chemists can exploit for selective reactions.
In the current market landscape, there's growing interest in fluorinated building blocks like butyl 2-fluoro-6-hydroxybenzoate, driven by the pharmaceutical industry's need for novel drug candidates. Approximately 30% of newly approved drugs contain fluorine atoms, highlighting the importance of such compounds. The agrochemical sector also shows increasing demand for fluorinated intermediates to develop more effective crop protection agents with lower environmental impact.
The synthesis of butyl 2-fluoro-6-hydroxybenzoate typically involves esterification reactions starting from 2-fluoro-6-hydroxybenzoic acid, with various catalytic methods being explored to improve yield and purity. Recent advances in green chemistry have led to more sustainable production methods, addressing industry concerns about environmental impact. These developments align with the broader chemical industry's shift toward sustainable synthesis practices.
Analytical characterization of butyl 2-fluoro-6-hydroxybenzoate typically employs techniques such as HPLC, NMR spectroscopy, and mass spectrometry. These methods confirm the compound's purity and structural integrity, which are crucial for research and industrial applications. The fluoro substituent in particular shows distinctive signals in 19F NMR analysis, providing valuable information for quality control.
Storage and handling of butyl 2-fluoro-6-hydroxybenzoate require standard laboratory precautions for organic compounds. While not classified as hazardous under normal conditions, proper storage in airtight containers away from strong oxidizers is recommended to maintain stability. The compound's shelf life can be extended by storing at low temperatures in amber glass containers, especially important for research applications requiring high-purity materials.
Looking toward future applications, researchers are exploring the potential of butyl 2-fluoro-6-hydroxybenzoate in material science, particularly in the development of specialty polymers and liquid crystals. The combination of fluorine and hydroxy groups offers interesting possibilities for creating materials with tailored surface properties and optical characteristics. This aligns with current trends in advanced materials development for electronics and coatings applications.
For researchers sourcing butyl 2-fluoro-6-hydroxybenzoate, it's important to verify the supplier's quality control processes and analytical data. The compound is typically available in research quantities from specialty chemical suppliers, with purity levels ranging from 95% to 99%. Recent market analysis shows steady growth in demand for such fine chemicals, particularly from contract research organizations and academic institutions engaged in medicinal chemistry programs.
In conclusion, butyl 2-fluoro-6-hydroxybenzoate (CAS No. 1056955-09-9) represents an important building block in modern organic synthesis, with growing applications across pharmaceutical and material science fields. Its unique combination of fluorine and hydroxy functionality continues to attract research interest, particularly in the development of novel bioactive compounds. As the chemical industry evolves toward more specialized and sustainable solutions, compounds like this will likely play an increasingly important role in scientific innovation.
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