Cas no 1989-73-7 (2-(4-hydroxy-3,5-dimethylphenyl)acetic acid)
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid Chemical and Physical Properties
Names and Identifiers
-
- Benzeneacetic acid,4-hydroxy-3,5-dimethyl-
- 2-(4-Hydroxy-3,5-dimethylphenyl)acetic acid
- 3,5-DIMETHYL-4-HYDROXYPHENYLACETIC ACID
- (3,5-dimethyl-4-hydroxy-phenyl)-acetic acid
- (4-hydroxy-3,5-dimethylphenyl)acetic acid
- (4-hydroxy-3,5-dimethylphenyl)-acetic acid
- (4-hydroxy-3,5-dimethyl-phenyl)-acetic acid
- (4-Hydroxy-3,5-dimethyl-phenyl)-essigsaeure
- 3,5-dimethyl-4-hydroxy-phenyl acetic acid
- 4-Hydroxy-3,5-dimethyl-phenylessigsaeure
- CTK4E2675
- SBB018840
- ST090665
- STK694418
- SureCN2921654
- 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid
-
- Inchi: 1S/C10H12O3/c1-6-3-8(5-9(11)12)4-7(2)10(6)13/h3-4,13H,5H2,1-2H3,(H,11,12)
- InChI Key: RINPNKCWFHYQHB-UHFFFAOYSA-N
- SMILES: OC1=C(C)C=C(CC(=O)O)C=C1C
Computed Properties
- Exact Mass: 180.07866
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 13
- Rotatable Bond Count: 2
Experimental Properties
- PSA: 57.53
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | D481970-1g |
3,5-Dimethyl-4-hydroxyphenylacetic acid |
1989-73-7 | 1g |
$ 50.00 | 2022-06-05 | ||
| TRC | D481970-5g |
3,5-Dimethyl-4-hydroxyphenylacetic acid |
1989-73-7 | 5g |
$ 135.00 | 2022-06-05 | ||
| TRC | D481970-10g |
3,5-Dimethyl-4-hydroxyphenylacetic acid |
1989-73-7 | 10g |
$ 210.00 | 2022-06-05 | ||
| Alichem | A010015357-250mg |
3,5-Dimethyl-4-hydroxyphenylacetic acid |
1989-73-7 | 97% | 250mg |
$499.20 | 2023-09-02 | |
| Alichem | A010015357-500mg |
3,5-Dimethyl-4-hydroxyphenylacetic acid |
1989-73-7 | 97% | 500mg |
$847.60 | 2023-09-02 | |
| Alichem | A010015357-1g |
3,5-Dimethyl-4-hydroxyphenylacetic acid |
1989-73-7 | 97% | 1g |
$1579.40 | 2023-09-02 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBTQ8048-100mg |
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid |
1989-73-7 | 95% | 100mg |
¥726.0 | 2024-04-22 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBTQ8048-250mg |
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid |
1989-73-7 | 95% | 250mg |
¥970.0 | 2024-04-22 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBTQ8048-500mg |
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid |
1989-73-7 | 95% | 500mg |
¥1617.0 | 2024-04-22 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBTQ8048-1g |
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid |
1989-73-7 | 95% | 1g |
¥2429.0 | 2024-04-22 |
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid Suppliers
2-(4-hydroxy-3,5-dimethylphenyl)acetic acid Related Literature
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Xue-Ying Wang,Ying Pei,Min Xie,Zi-He Jin,Ya-Shi Xiao,Yang Wang,Li-Na Zhang,Yan Li,Wei-Hua Huang Lab Chip, 2015,15, 1178-1187
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Xiaofeng Lin RSC Adv., 2016,6, 9002-9006
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Priyambada Nayak,Tanmaya Badapanda,Anil Kumar Singh,Simanchalo Panigrahi RSC Adv., 2017,7, 16319-16331
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R. M. Pemberton,J. P. Hart,T. T. Mottram Analyst, 2001,126, 1866-1871
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J. M. Granadino-Roldán,M. Fernández-Gómez,A. Navarro,T. Pe?a Ruiz,U. A. Jayasooriya Phys. Chem. Chem. Phys., 2004,6, 1133-1143
Additional information on 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid
Exploring the Versatile Applications of 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid (CAS No. 1989-73-7) in Modern Chemistry
In the realm of fine chemicals and pharmaceutical intermediates, 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid (CAS 1989-73-7) stands out as a compound of significant interest. This aromatic carboxylic acid, characterized by its hydroxyl and dimethyl substitutions, has garnered attention for its unique chemical properties and broad utility across multiple industries. As researchers increasingly focus on sustainable and efficient chemical processes, understanding this compound's potential becomes crucial for innovation in material science and drug development.
The molecular structure of 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid features a phenylacetic acid backbone with strategic substitutions that enhance its reactivity and functionality. The presence of both electron-donating methyl groups and an acidic hydroxyl group creates interesting electronic effects that influence its behavior in synthetic applications. These structural characteristics make it particularly valuable as a building block in organic synthesis, where precise control over molecular architecture is paramount.
Recent advancements in green chemistry have highlighted the importance of compounds like 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid (CAS 1989-73-7) that can serve as eco-friendly alternatives in various processes. Its potential as a precursor for biodegradable materials aligns with current environmental concerns and the push toward sustainable industrial practices. Researchers are particularly interested in its role in developing novel pharmaceutical intermediates with reduced environmental impact.
In pharmaceutical applications, this compound has shown promise as a key intermediate in the synthesis of various bioactive molecules. The presence of both phenolic and carboxylic acid functional groups allows for diverse chemical modifications, making it valuable for creating libraries of potential drug candidates. Current studies explore its utility in developing compounds with potential anti-inflammatory and antioxidant properties, addressing growing health concerns in modern society.
The material science field has also recognized the value of 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid. Its structural features make it suitable for incorporation into advanced polymers and functional materials. Researchers are investigating its use in creating high-performance coatings and specialty adhesives, particularly where thermal stability and chemical resistance are required. These applications respond to industry demands for more durable and efficient materials.
From a synthetic chemistry perspective, the compound's regioselective reactivity offers advantages in multi-step synthesis processes. The hydroxyl group at the para position, flanked by methyl groups, provides steric protection that can be exploited for selective functionalization. This characteristic is particularly valuable in complex molecule construction, where control over reaction pathways is essential.
Market trends indicate growing demand for 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid (CAS 1989-73-7) as industries seek more specialized chemical building blocks. The compound's versatility supports its use across pharmaceuticals, agrochemicals, and material science, creating diverse opportunities for manufacturers and researchers alike. Current production methods continue to evolve, with emphasis on cost-effective and environmentally benign synthetic routes.
Analytical characterization of this compound presents interesting challenges and opportunities. The interplay between its aromatic system, hydrogen bonding capacity, and acid-base properties requires sophisticated analytical techniques for complete characterization. Modern spectroscopic methods, including NMR and mass spectrometry, are essential tools for quality control and research applications involving this material.
Future research directions for 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid are likely to focus on expanding its applications in medicinal chemistry and functional materials. The compound's structural features suggest potential in developing new classes of therapeutic agents and smart materials. Additionally, as computational chemistry advances, predictive modeling may reveal novel applications for this versatile building block in emerging technologies.
For researchers and industry professionals seeking reliable information about 2-(4-hydroxy-3,5-dimethylphenyl)acetic acid (CAS 1989-73-7), understanding its physicochemical properties, synthetic utility, and commercial availability is essential. This compound represents an excellent example of how strategically functionalized aromatic acids continue to play vital roles in advancing chemical science and industrial applications.
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