Cas no 22890-53-5 (4-ethyl-2-hydroxybenzoic acid)
4-ethyl-2-hydroxybenzoic acid Chemical and Physical Properties
Names and Identifiers
-
- Benzoic acid,4-ethyl-2-hydroxy-
- 4-ethyl-2-hydroxybenzoic acid
- 2-hydroxy-4-ethylbenzoic acid
- 4-Aethyl-2-hydroxy-benzoesaeure
- 4-Et-2-OHC6H3CO2H
- 4-Ethyl-2-hydroxy-benzoic acid
- 4-ethylsalicylic acid
- 4-Ethylsalicylsaeure
- AC1L65QK
- AC1Q5TZ4
- AR-1G2212
- CTK4F0394
- NCIOpen2_001392
- NSC94405
- SureCN2126940
-
- Inchi: 1S/C9H10O3/c1-2-6-3-4-7(9(11)12)8(10)5-6/h3-5,10H,2H2,1H3,(H,11,12)
- InChI Key: GGSAASVFCYXBCT-UHFFFAOYSA-N
- SMILES: OC1=C(C(=O)O)C=CC(=C1)CC
Computed Properties
- Exact Mass: 166.063
Experimental Properties
- PSA: 57.53
- LogP: 1.65280
4-ethyl-2-hydroxybenzoic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B440468-10mg |
4-ethyl-2-hydroxybenzoic acid |
22890-53-5 | 10mg |
$ 50.00 | 2022-06-01 | ||
| TRC | B440468-50mg |
4-ethyl-2-hydroxybenzoic acid |
22890-53-5 | 50mg |
$ 210.00 | 2022-06-01 | ||
| TRC | B440468-100mg |
4-ethyl-2-hydroxybenzoic acid |
22890-53-5 | 100mg |
$ 295.00 | 2022-06-01 | ||
| Alichem | A010000096-250mg |
4-Ethyl-2-hydroxybenzoic acid |
22890-53-5 | 97% | 250mg |
$470.40 | 2023-09-02 | |
| Alichem | A010000096-500mg |
4-Ethyl-2-hydroxybenzoic acid |
22890-53-5 | 97% | 500mg |
$863.90 | 2023-09-02 | |
| Alichem | A010000096-1g |
4-Ethyl-2-hydroxybenzoic acid |
22890-53-5 | 97% | 1g |
$1504.90 | 2023-09-02 | |
| A2B Chem LLC | AB20793-10g |
4-Ethyl-2-hydroxybenzoic acid |
22890-53-5 | 95% | 10g |
$3589.00 | 2024-04-20 | |
| A2B Chem LLC | AB20793-50mg |
4-Ethyl-2-hydroxybenzoic acid |
22890-53-5 | 95% | 50mg |
$227.00 | 2024-04-20 | |
| A2B Chem LLC | AB20793-100mg |
4-Ethyl-2-hydroxybenzoic acid |
22890-53-5 | 95% | 100mg |
$322.00 | 2024-04-20 | |
| A2B Chem LLC | AB20793-250mg |
4-Ethyl-2-hydroxybenzoic acid |
22890-53-5 | 95% | 250mg |
$445.00 | 2024-04-20 |
4-ethyl-2-hydroxybenzoic acid Related Literature
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Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
-
Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
Additional information on 4-ethyl-2-hydroxybenzoic acid
Benzoic acid,4-ethyl-2-hydroxy- (CAS No. 22890-53-5): A Comprehensive Overview
Benzoic acid,4-ethyl-2-hydroxy-, identified by its Chemical Abstracts Service (CAS) number CAS No. 22890-53-5, is a compound of significant interest in the field of chemical and pharmaceutical research. This molecule, characterized by its unique structural and functional properties, has garnered attention due to its potential applications in various scientific domains. The compound's molecular structure, featuring a benzoic acid backbone with ethyl and hydroxyl substituents, contributes to its diverse chemical behavior and reactivity.
The synthesis and characterization of Benzoic acid,4-ethyl-2-hydroxy- involve meticulous chemical processes that highlight the compound's versatility. The presence of the hydroxyl group at the 2-position and the ethyl group at the 4-position introduces both polar and non-polar characteristics to the molecule, making it a valuable candidate for further functionalization and derivatization. These structural features are crucial in determining its interactions with biological systems, which has implications for its potential use in pharmaceuticals and agrochemicals.
In recent years, there has been growing interest in exploring the pharmacological properties of Benzoic acid,4-ethyl-2-hydroxy-. Research has indicated that this compound exhibits promising activities as an antioxidant and anti-inflammatory agent. The hydroxyl group, in particular, plays a pivotal role in these biological activities by facilitating hydrogen bonding interactions with target molecules. Furthermore, the ethyl group contributes to the molecule's lipophilicity, enhancing its ability to penetrate biological membranes.
One of the most intriguing aspects of Benzoic acid,4-ethyl-2-hydroxy- is its potential as a precursor in drug development. The benzoic acid core is a well-known scaffold in medicinal chemistry, with numerous drugs derived from it demonstrating efficacy in treating various conditions. The introduction of ethyl and hydroxyl groups modifies the electronic properties of the molecule, allowing for fine-tuning of its pharmacological profile. This flexibility makes it an attractive candidate for designing novel therapeutic agents.
The compound's role in chemical biology has also been extensively studied. Researchers have investigated its interactions with enzymes and receptors, uncovering mechanisms that could lead to new treatment strategies. For instance, studies have shown that derivatives of Benzoic acid,4-ethyl-2-hydroxy- can modulate the activity of certain enzymes involved in metabolic pathways. This finding opens up possibilities for developing drugs that target metabolic disorders.
Moreover, the environmental impact of Benzoic acid,4-ethyl-2-hydroxy- has been a subject of interest. Its degradation products and ecological persistence are critical factors to consider when evaluating its suitability for industrial applications. Recent studies have demonstrated that under certain conditions, this compound can be biodegraded by microorganisms, suggesting a relatively low environmental risk. However, further research is needed to fully understand its long-term ecological effects.
The synthetic pathways for producing Benzoic acid,4-ethyl-2-hydroxy- have been optimized to ensure high yield and purity. Advanced techniques such as catalytic hydrogenation and selective oxidation are employed to introduce the desired functional groups efficiently. These synthetic methods not only highlight the compound's synthetic utility but also contribute to the broader field of organic chemistry by providing new insights into molecular construction.
In conclusion, Benzoic acid,4-ethyl-2-hydroxy-, with its CAS number CAS No. 22890-53-5, represents a fascinating subject of study in chemical biology and pharmaceutical research. Its unique structural features and diverse biological activities make it a valuable compound for further exploration. As research continues to uncover new applications and mechanisms associated with this molecule, it is likely to play an increasingly important role in drug development and other scientific endeavors.
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