Cas no 10419-34-8 (2-2-(Methylsulfanyl)phenylacetic Acid)
2-2-(Methylsulfanyl)phenylacetic Acid Chemical and Physical Properties
Names and Identifiers
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- Benzeneacetic acid, 2-(methylthio)-
- 2-(2-methylsulfanylphenyl)acetic acid
- 2-2-(Methylsulfanyl)phenylacetic Acid
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- MDL: MFCD11898922
- Inchi: 1S/C9H10O2S/c1-12-8-5-3-2-4-7(8)6-9(10)11/h2-5H,6H2,1H3,(H,10,11)
- InChI Key: PSRVZRJMWNFSIZ-UHFFFAOYSA-N
- SMILES: S(C)C1C=CC=CC=1CC(=O)O
Computed Properties
- Exact Mass: 182.0402
Experimental Properties
- PSA: 37.3
2-2-(Methylsulfanyl)phenylacetic Acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B487233-10mg |
2-[2-(Methylsulfanyl)phenyl]acetic Acid |
10419-34-8 | 10mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B487233-50mg |
2-[2-(Methylsulfanyl)phenyl]acetic Acid |
10419-34-8 | 50mg |
$ 115.00 | 2022-06-07 | ||
| TRC | B487233-100mg |
2-[2-(Methylsulfanyl)phenyl]acetic Acid |
10419-34-8 | 100mg |
$ 185.00 | 2022-06-07 | ||
| Enamine | EN300-127131-0.05g |
2-[2-(methylsulfanyl)phenyl]acetic acid |
10419-34-8 | 95.0% | 0.05g |
$55.0 | 2025-02-21 | |
| Enamine | EN300-127131-0.1g |
2-[2-(methylsulfanyl)phenyl]acetic acid |
10419-34-8 | 95.0% | 0.1g |
$81.0 | 2025-02-21 | |
| Enamine | EN300-127131-0.25g |
2-[2-(methylsulfanyl)phenyl]acetic acid |
10419-34-8 | 95.0% | 0.25g |
$115.0 | 2025-02-21 | |
| Enamine | EN300-127131-0.5g |
2-[2-(methylsulfanyl)phenyl]acetic acid |
10419-34-8 | 95.0% | 0.5g |
$182.0 | 2025-02-21 | |
| Enamine | EN300-127131-1.0g |
2-[2-(methylsulfanyl)phenyl]acetic acid |
10419-34-8 | 95.0% | 1.0g |
$233.0 | 2025-02-21 | |
| Enamine | EN300-127131-2.5g |
2-[2-(methylsulfanyl)phenyl]acetic acid |
10419-34-8 | 95.0% | 2.5g |
$457.0 | 2025-02-21 | |
| Enamine | EN300-127131-5.0g |
2-[2-(methylsulfanyl)phenyl]acetic acid |
10419-34-8 | 95.0% | 5.0g |
$675.0 | 2025-02-21 |
2-2-(Methylsulfanyl)phenylacetic Acid Related Literature
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Bo Wei,Zhenyu Liu,Chen Xie,Shu Yang,Wentao Tang,Aiwei Gu,Wing-Tak Wong,Ka-Leung Wong J. Mater. Chem. C, 2015,3, 12322-12327
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Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
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Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431
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Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
Additional information on 2-2-(Methylsulfanyl)phenylacetic Acid
Introduction to 2-2-(Methylsulfanyl)phenylacetic Acid (CAS No. 10419-34-8) and Its Emerging Applications in Chemical Biology
2-2-(Methylsulfanyl)phenylacetic acid, identified by the Chemical Abstracts Service Number (CAS No.) 10419-34-8, is a specialized organic compound that has garnered significant attention in the field of chemical biology due to its unique structural and functional properties. This compound, featuring a phenyl ring substituted with a methylsulfanyl group and an acetic acid moiety, exhibits promising characteristics that make it a valuable candidate for various biochemical and pharmaceutical applications. The molecular structure of this compound not only contributes to its reactivity but also opens up avenues for innovative research in drug discovery and molecular therapy.
The methylsulfanyl group in the molecule introduces a polar nature, enhancing its solubility in both aqueous and organic solvents, which is a critical factor for its utility in formulation development. This dual solubility profile allows for versatile applications, ranging from in vitro assays to potential in vivo studies. Furthermore, the presence of the phenylacetic acid backbone suggests potential interactions with biological targets such as enzymes and receptors, making it an intriguing candidate for modulating biological pathways.
In recent years, there has been a surge in research focusing on phenylacetic acid derivatives due to their reported bioactivities. Studies have demonstrated that compounds structurally related to 2-2-(methylsulfanyl)phenylacetic acid may possess properties relevant to neuroprotective, anti-inflammatory, and even anticancer effects. For instance, modifications of the phenyl ring or the acetic acid side chain can lead to compounds with enhanced binding affinity to specific targets. The methylsulfanyl moiety, in particular, has been shown to influence the electronic properties of the aromatic ring, potentially affecting how the molecule interacts with biological systems.
One of the most compelling aspects of 2-2-(methylsulfanyl)phenylacetic acid is its potential as a scaffold for drug design. Researchers are exploring its ability to serve as a precursor for more complex molecules that could be tailored for specific therapeutic purposes. The compound’s versatility allows chemists to introduce additional functional groups or modify existing ones to fine-tune its pharmacological profile. This adaptability is particularly valuable in medicinal chemistry, where optimizing drug candidates often involves iterative modifications based on structural and functional data.
The chemical biology community has also been interested in understanding how 2-2-(methylsulfanyl)phenylacetic acid behaves within complex systems. Preliminary studies suggest that this compound may influence cellular processes by interacting with intracellular signaling pathways. For example, its ability to modulate the activity of certain enzymes or receptors could have implications for treating diseases associated with dysregulated signaling. Additionally, the compound’s stability under various conditions makes it suitable for long-term studies aimed at elucidating its mechanisms of action.
From a synthetic chemistry perspective, 2-2-(methylsulfanyl)phenylacetic acid (CAS No. 10419-34-8) represents an interesting challenge due to its structural complexity. The synthesis of this compound requires careful consideration of reaction conditions and purification techniques to ensure high yield and purity. Advances in synthetic methodologies have enabled more efficient production processes, allowing researchers to access larger quantities of this compound for further investigation. These improvements are crucial for supporting both academic research and industrial development efforts.
The pharmaceutical industry has taken note of the potential applications of 2-2-(methylsulfanyl)phenylacetic acid derivatives. Companies are investing in research programs aimed at identifying novel therapeutic agents based on similar chemical structures. The compound’s ability to interact with multiple biological targets makes it an attractive candidate for developing multitarget drugs, which can offer broader therapeutic benefits with fewer side effects compared to single-target agents.
In conclusion, 2-2-(methylsulfanyl)phenylacetic acid (CAS No. 10419-34-8) is a multifaceted compound with significant potential in chemical biology and pharmaceutical research. Its unique structure, combined with its reported bioactivities, positions it as a valuable tool for drug discovery and molecular therapy. As research continues to uncover new applications and mechanisms associated with this compound, it is likely to remain a key focus area for scientists seeking innovative solutions in medicine and biotechnology.
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