Cas no 1158310-32-7 ((4-FLUORO-1H-INDOL-3-YL)METHANOL)
(4-FLUORO-1H-INDOL-3-YL)METHANOL Chemical and Physical Properties
Names and Identifiers
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- (4-FLUORO-1H-INDOL-3-YL)METHANOL
- CHEMBL4557387
- AKOS017515519
- 1158310-32-7
- EN300-187026
-
- Inchi: 1S/C9H8FNO/c10-7-2-1-3-8-9(7)6(5-12)4-11-8/h1-4,11-12H,5H2
- InChI Key: YOJTVZBCNRZWDJ-UHFFFAOYSA-N
- SMILES: FC1=CC=CC2=C1C(CO)=CN2
Computed Properties
- Exact Mass: 165.058992041g/mol
- Monoisotopic Mass: 165.058992041g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 12
- Rotatable Bond Count: 1
- Complexity: 165
- 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
- XLogP3: 1.4
- Topological Polar Surface Area: 36?2
(4-FLUORO-1H-INDOL-3-YL)METHANOL Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | F592668-5mg |
(4-Fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 5mg |
$ 50.00 | 2022-06-04 | ||
| TRC | F592668-10mg |
(4-Fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 10mg |
$ 70.00 | 2022-06-04 | ||
| TRC | F592668-50mg |
(4-Fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 50mg |
$ 295.00 | 2022-06-04 | ||
| Enamine | EN300-187026-1.0g |
(4-fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 95% | 1g |
$0.0 | 2023-06-08 | |
| Enamine | EN300-187026-0.05g |
(4-fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 95% | 0.05g |
$229.0 | 2023-09-18 | |
| Enamine | EN300-187026-0.1g |
(4-fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 95% | 0.1g |
$342.0 | 2023-09-18 | |
| Enamine | EN300-187026-0.25g |
(4-fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 95% | 0.25g |
$487.0 | 2023-09-18 | |
| Enamine | EN300-187026-0.5g |
(4-fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 95% | 0.5g |
$768.0 | 2023-09-18 | |
| Enamine | EN300-187026-1g |
(4-fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 95% | 1g |
$986.0 | 2023-09-18 | |
| Enamine | EN300-187026-2.5g |
(4-fluoro-1H-indol-3-yl)methanol |
1158310-32-7 | 95% | 2.5g |
$1931.0 | 2023-09-18 |
(4-FLUORO-1H-INDOL-3-YL)METHANOL Related Literature
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre Albrecht Chem. Commun., 2001, 1976-1977
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
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Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
Additional information on (4-FLUORO-1H-INDOL-3-YL)METHANOL
Compound CAS No. 1158310-32-7: (4-Fluoro-1H-indol-3-yl)methanol
(4-Fluoro-1H-indol-3-yl)methanol, also known by its CAS number 1158310-32-7, is a fascinating compound that has garnered significant attention in the fields of organic chemistry and pharmacology. This compound belongs to the class of indole derivatives, which are known for their diverse biological activities and structural versatility. The presence of a fluorine atom at the 4-position of the indole ring introduces unique electronic and steric properties, making this compound particularly interesting for various applications.
The molecular structure of (4-fluoroindolyl)methanol consists of an indole ring system with a fluorine substituent at position 4 and a hydroxymethyl group (-CH?OH) attached at position 3. This arrangement not only enhances the compound's stability but also provides opportunities for further functionalization. Recent studies have highlighted the potential of this compound in drug discovery, particularly in the development of anticancer agents and neuroprotective drugs.
One of the most notable aspects of CAS No. 1158310-32-7 is its ability to act as a precursor in the synthesis of more complex molecules. For instance, researchers have utilized this compound as a starting material for constructing bioactive compounds with improved pharmacokinetic profiles. The hydroxymethyl group serves as a reactive site, enabling various chemical transformations such as oxidation, reduction, and coupling reactions.
Recent advancements in synthetic methodologies have made it possible to produce (4-fluoroindolyl)methanol in high yields and with excellent purity. These methods often involve multi-step synthesis strategies that incorporate fluorination techniques and stereochemical control. The use of microwave-assisted synthesis has also been reported, significantly reducing reaction times while maintaining product quality.
In terms of biological activity, CAS No. 1158310-32-7 has shown promising results in vitro against several cancer cell lines. Studies indicate that the compound exhibits selective cytotoxicity, potentially due to its ability to modulate key cellular pathways involved in apoptosis and cell proliferation. Additionally, preliminary animal studies suggest that this compound may have neuroprotective effects, making it a candidate for treating neurodegenerative diseases such as Alzheimer's disease.
The pharmacokinetic properties of (4-fluoroindolyl)methanol have also been investigated. Research findings reveal that the compound demonstrates moderate absorption and distribution characteristics, with a favorable half-life profile. These attributes make it a viable candidate for further preclinical testing and eventual clinical trials.
In conclusion, CAS No. 1158310-32-7, or (4-fluoroindolyl)methanol, represents a valuable addition to the arsenal of bioactive compounds available for drug discovery. Its unique structure, coupled with its promising biological activity, positions it as a potential lead molecule for developing innovative therapeutic agents. As research continues to uncover its full potential, this compound is likely to play an increasingly important role in advancing medical science.
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