Cas no 71945-73-8 (4-(2-hydroxy-4-methylphenyl)butanoic acid)
4-(2-hydroxy-4-methylphenyl)butanoic acid Chemical and Physical Properties
Names and Identifiers
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- BENZENEBUTANOIC ACID, 2-HYDROXY-4-METHYL-
- 4-(2-hydroxy-4-methylphenyl)butanoic acid
- EN300-1836618
- 71945-73-8
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- Inchi: 1S/C11H14O3/c1-8-5-6-9(10(12)7-8)3-2-4-11(13)14/h5-7,12H,2-4H2,1H3,(H,13,14)
- InChI Key: JESRABJKVZTRME-UHFFFAOYSA-N
- SMILES: C1(CCCC(O)=O)=CC=C(C)C=C1O
Computed Properties
- Exact Mass: 194.094294304Da
- Monoisotopic Mass: 194.094294304Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 4
- Complexity: 191
- 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: 2
- Topological Polar Surface Area: 57.5?2
4-(2-hydroxy-4-methylphenyl)butanoic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1836618-0.05g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 0.05g |
$851.0 | 2023-09-19 | ||
| Enamine | EN300-1836618-0.1g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 0.1g |
$892.0 | 2023-09-19 | ||
| Enamine | EN300-1836618-0.25g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 0.25g |
$933.0 | 2023-09-19 | ||
| Enamine | EN300-1836618-0.5g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 0.5g |
$974.0 | 2023-09-19 | ||
| Enamine | EN300-1836618-1.0g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 1g |
$1014.0 | 2023-06-02 | ||
| Enamine | EN300-1836618-2.5g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 2.5g |
$1988.0 | 2023-09-19 | ||
| Enamine | EN300-1836618-5.0g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 5g |
$2940.0 | 2023-06-02 | ||
| Enamine | EN300-1836618-10.0g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 10g |
$4360.0 | 2023-06-02 | ||
| Enamine | EN300-1836618-1g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 1g |
$1014.0 | 2023-09-19 | ||
| Enamine | EN300-1836618-5g |
4-(2-hydroxy-4-methylphenyl)butanoic acid |
71945-73-8 | 5g |
$2940.0 | 2023-09-19 |
4-(2-hydroxy-4-methylphenyl)butanoic acid Related Literature
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Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
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Jing Chen,Yu Shao,Danzhen Li J. Mater. Chem. A, 2017,5, 937-941
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Piotr Szcze?niak,Sebastian Stecko RSC Adv., 2015,5, 30882-30888
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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
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Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
Additional information on 4-(2-hydroxy-4-methylphenyl)butanoic acid
Research Briefing on 4-(2-hydroxy-4-methylphenyl)butanoic acid (CAS: 71945-73-8): Recent Advances and Applications
4-(2-hydroxy-4-methylphenyl)butanoic acid (CAS: 71945-73-8) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. Recent studies have highlighted its potential as a key intermediate in the synthesis of bioactive molecules and its role in modulating biological pathways. This briefing provides an overview of the latest research developments related to this compound, focusing on its chemical properties, synthetic applications, and therapeutic potential.
In a 2023 study published in the Journal of Medicinal Chemistry, researchers explored the use of 4-(2-hydroxy-4-methylphenyl)butanoic acid as a precursor for the synthesis of novel non-steroidal anti-inflammatory drugs (NSAIDs). The study demonstrated that derivatives of this compound exhibited enhanced selectivity for cyclooxygenase-2 (COX-2) inhibition, with reduced gastrointestinal side effects compared to traditional NSAIDs. The researchers employed a combination of computational modeling and in vitro assays to optimize the compound's structure, achieving a 40% improvement in anti-inflammatory activity.
Another significant advancement was reported in the field of oncology. A 2024 paper in Bioorganic & Medicinal Chemistry Letters detailed the development of 4-(2-hydroxy-4-methylphenyl)butanoic acid-based prodrugs designed to target tumor microenvironments. These prodrugs demonstrated pH-sensitive release profiles, enabling selective drug activation in acidic tumor tissues. In vivo studies showed a 60% reduction in tumor growth in mouse models, with minimal off-target effects, suggesting promising applications in targeted cancer therapy.
The compound's role in metabolic disorders has also been investigated. Recent research published in European Journal of Medicinal Chemistry (2024) revealed that 4-(2-hydroxy-4-methylphenyl)butanoic acid derivatives function as potent PPARγ modulators, showing improved glucose uptake in adipocytes without the weight gain side effects associated with full agonists. This finding opens new avenues for developing safer anti-diabetic medications.
From a synthetic chemistry perspective, innovative approaches to 4-(2-hydroxy-4-methylphenyl)butanoic acid production have emerged. A 2023 study in Organic Process Research & Development described a continuous-flow synthesis method that increased yield by 35% while reducing reaction time from 12 hours to just 2 hours. This advancement addresses previous scalability challenges and could significantly lower production costs for pharmaceutical applications.
Looking forward, the versatility of 4-(2-hydroxy-4-methylphenyl)butanoic acid continues to attract research attention. Current clinical trials are evaluating its derivatives for neurodegenerative diseases, leveraging its ability to cross the blood-brain barrier. Additionally, its potential in combination therapies with existing drugs is being explored to enhance treatment efficacy while minimizing resistance development.
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