Cas no 63987-19-9 (4'-Hydroxy-3-phenoxybenzyl Alcohol)
4'-Hydroxy-3-phenoxybenzyl Alcohol Chemical and Physical Properties
Names and Identifiers
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- Benzenemethanol,3-(4-hydroxyphenoxy)-
- 4′-Hydroxy-3-phenoxybenzyl Alcohol
- 4?-Hydroxy-3-phenoxybenzyl Alcohol
- 4-[3-(Hydroxymethyl)phenoxy]phenol
- 4'-Hydroxy-3-phenoxybenzyl Alcohol
- RO3280
- 3-[(4-hydroxy)phenoxy]benzyl alcohol
- Benzenemethanol, 3-(4-hydroxyphenoxy)-
- SCHEMBL5112767
- NS00124377
- 4-(3-(Hydroxymethyl)phenoxy)phenol
- DTXSID70981711
- 3-(4-Hydroxyphenoxy)benzenemethanol
- F14701
- 63987-19-9
-
- Inchi: 1S/C13H12O3/c14-9-10-2-1-3-13(8-10)16-12-6-4-11(15)5-7-12/h1-8,14-15H,9H2
- InChI Key: PJOAGCNCAOJNKZ-UHFFFAOYSA-N
- SMILES: O(C1C=CC(=CC=1)O)C1=CC=CC(CO)=C1
Computed Properties
- Exact Mass: 216.07900
- Monoisotopic Mass: 216.079
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 16
- Rotatable Bond Count: 3
- Complexity: 199
- 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: 2.1
- Topological Polar Surface Area: 49.7A^2
Experimental Properties
- Density: 1.3±0.1 g/cm3
- Boiling Point: 398.2±32.0 °C at 760 mmHg
- Flash Point: 194.6±25.1 °C
- Refractive Index: 1.626
- PSA: 49.69000
- LogP: 2.67680
- Vapor Pressure: 0.0±1.0 mmHg at 25°C
4'-Hydroxy-3-phenoxybenzyl Alcohol Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
4'-Hydroxy-3-phenoxybenzyl Alcohol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | H951235-5mg |
4'-Hydroxy-3-phenoxybenzyl Alcohol |
63987-19-9 | 5mg |
$196.00 | 2023-05-18 | ||
| TRC | H951235-50mg |
4'-Hydroxy-3-phenoxybenzyl Alcohol |
63987-19-9 | 50mg |
$1533.00 | 2023-05-18 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-210196-5 mg |
4'-Hydroxy-3-phenoxybenzyl Alcohol, |
63987-19-9 | ≥98% | 5mg |
¥3,046.00 | 2023-07-11 | |
| SHENG KE LU SI SHENG WU JI SHU | sc-210196-5mg |
4'-Hydroxy-3-phenoxybenzyl Alcohol, |
63987-19-9 | ≥98% | 5mg |
¥3046.00 | 2023-09-05 | |
| TRC | H951235-100mg |
4'-Hydroxy-3-phenoxybenzyl Alcohol |
63987-19-9 | 100mg |
$ 3000.00 | 2023-09-07 | ||
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1651169-1g |
4-(3-(Hydroxymethyl)phenoxy)phenol |
63987-19-9 | 98% | 1g |
¥7980.00 | 2024-05-05 | |
| Crysdot LLC | CD12048639-1g |
4-(3-(Hydroxymethyl)phenoxy)phenol |
63987-19-9 | 97% | 1g |
$887 | 2024-07-18 |
4'-Hydroxy-3-phenoxybenzyl Alcohol Related Literature
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Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
Additional information on 4'-Hydroxy-3-phenoxybenzyl Alcohol
Professional Introduction to 4'-Hydroxy-3-phenoxybenzyl Alcohol (CAS No. 63987-19-9)
4'-Hydroxy-3-phenoxybenzyl Alcohol, chemically designated as 4'-Hydroxy-3-phenoxybenzyl Alcohol, is a significant compound in the realm of pharmaceutical chemistry and bioorganic synthesis. With the CAS number CAS No. 63987-19-9, this molecule has garnered attention due to its versatile structural features and potential applications in drug development. The compound’s unique aromatic and hydroxyl functionalities make it a valuable intermediate in the synthesis of various pharmacologically active agents.
The< strong>4'-Hydroxy-3-phenoxybenzyl Alcohol molecule consists of a benzene ring substituted with both a hydroxyl group and a phenoxy side chain. This structural configuration imparts distinct chemical properties that are highly relevant in medicinal chemistry. The presence of the hydroxyl group enhances its solubility in polar solvents, while the phenoxy moiety contributes to its interaction with biological targets. Such characteristics have positioned this compound as a candidate for further exploration in the development of novel therapeutic agents.
In recent years, there has been a growing interest in natural product-inspired scaffolds for drug discovery. The< strong>4'-Hydroxy-3-phenoxybenzyl Alcohol structure bears resemblance to several bioactive molecules found in plants and microorganisms, suggesting potential pharmacological relevance. Researchers have been investigating its derivatives as candidates for antimicrobial, anti-inflammatory, and anticancer applications. The hydroxyl group’s ability to participate in hydrogen bonding interactions with biological targets makes it particularly useful in designing molecules with enhanced binding affinity.
The< strong>CAS No. 63987-19-9 identification ensures precise chemical characterization and regulatory compliance, which are crucial for pharmaceutical applications. The compound’s synthesis involves multi-step organic reactions, often requiring careful control of reaction conditions to achieve high yields and purity. Advances in synthetic methodologies have enabled more efficient production processes, making< strong>4'-Hydroxy-3-phenoxybenzyl Alcohol more accessible for research and industrial purposes.
One of the most compelling aspects of< strong>4'-Hydroxy-3-phenoxybenzyl Alcohol is its role as a building block in medicinal chemistry. Its structural features allow for modifications that can fine-tune its pharmacological properties. For instance, introducing additional functional groups or altering the substitution pattern can lead to compounds with improved efficacy or reduced toxicity. Such flexibility makes it an attractive candidate for structure-activity relationship (SAR) studies.
The< strong>CAS No. 63987-19-9-determined compound has also found utility in the development of enzyme inhibitors. The hydroxyl and phenoxy groups provide multiple interaction points with enzymatic active sites, making it possible to design molecules that selectively target specific enzymes involved in disease pathways. This has been particularly relevant in the search for new treatments for metabolic disorders and neurological conditions.
In conclusion, 4'-Hydroxy-3-phenoxybenzyl Alcohol (CAS No. 63987-19-9) represents a promising compound with diverse applications in pharmaceutical research and drug development. Its unique structural features and potential biological activities make it a valuable asset in the quest for novel therapeutic agents. As research continues to uncover new synthetic strategies and pharmacological insights, the significance of this compound is expected to grow further.
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