Cas no 40232-88-0 (4-Benzyloxy-3-methoxyphenol)
4-Benzyloxy-3-methoxyphenol Chemical and Physical Properties
Names and Identifiers
-
- 4-Benzyloxy-3-methoxyphenol
- 3-methoxy-4-phenylmethoxyphenol
- Phenol,3-methoxy-4-(phenylmethoxy)-
- 3-Methoxy-4-(phenylmethoxy)phenol
- 3-Methoxy-4-benzyloxyphenol
- 4-(Benzyloxy)-3-methoxyphenol
- EN300-1861379
- FT-0662952
- DTXSID30340224
- SCHEMBL6881536
- C75037
- 4-(Benzyloxy)-3-methoxyphenol #
- AKOS027447872
- 40232-88-0
- Phenol, 3-methoxy-4-(phenylmethoxy)-
-
- Inchi： 1S/C14H14O3/c1-16-14-9-12(15)7-8-13(14)17-10-11-5-3-2-4-6-11/h2-9,15H,10H2,1H3
- InChI Key： ATQAGTXPLZDYGP-UHFFFAOYSA-N
- SMILES： O(C1C=CC(=CC=1OC)O)CC1C=CC=CC=1
Computed Properties
- Exact Mass: 230.09400
- Monoisotopic Mass: 230.094294304g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 17
- Rotatable Bond Count: 4
- Complexity: 214
- 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: 3
- Topological Polar Surface Area: 38.7?2
Experimental Properties
- Melting Point: 76-78°C
- Solubility: Chloroform(Slightly), Methanol (Slightly)
- PSA: 38.69000
- LogP: 2.97980
4-Benzyloxy-3-methoxyphenol Customs Data
- HS CODE：2909500000
- Customs Data：
China Customs Code:
2909500000Overview:
2909500000. Ether phenol\Ether alcohol phenol and its halogenation\sulfonation\Nitrosative or nitrosative derivatives. VAT:17.0%. Tax refund rate:9.0%. Regulatory conditions:nothing. MFN tariff:5.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2909500000 ether-phenols, ether-alcohol-phenols and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
4-Benzyloxy-3-methoxyphenol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B286515-1g |
4-Benzyloxy-3-methoxyphenol |
40232-88-0 | 1g |
$ 222.00 | 2023-04-18 | ||
| TRC | B286515-5g |
4-Benzyloxy-3-methoxyphenol |
40232-88-0 | 5g |
$ 965.00 | 2023-04-18 | ||
| TRC | B286515-10g |
4-Benzyloxy-3-methoxyphenol |
40232-88-0 | 10g |
$ 1654.00 | 2023-04-18 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | SF880-5g |
4-(Benzyloxy)-3-methoxyphenol |
40232-88-0 | 97% | 5g |
12476CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | SF880-25g |
4-(Benzyloxy)-3-methoxyphenol |
40232-88-0 | 97% | 25g |
31196CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | SF880-100mg |
4-(Benzyloxy)-3-methoxyphenol |
40232-88-0 | 97% | 100mg |
1301CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | SF880-1g |
4-(Benzyloxy)-3-methoxyphenol |
40232-88-0 | 97% | 1g |
5204CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | SF880-250mg |
4-(Benzyloxy)-3-methoxyphenol |
40232-88-0 | 97% | 250mg |
2077CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | SF880-10g |
4-(Benzyloxy)-3-methoxyphenol |
40232-88-0 | 97% | 10g |
18720CNY | 2021-05-07 | |
| Alichem | A019140788-5g |
4-(Benzyloxy)-3-methoxyphenol |
40232-88-0 | 97% | 5g |
$1575.84 | 2023-09-02 |
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4-Benzyloxy-3-methoxyphenol Related Literature
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1. 300. The constitution and synthesis of afromosinT. B. H. McMurry,C. Y. Theng J. Chem. Soc. 1960 1491
Additional information on 4-Benzyloxy-3-methoxyphenol
Professional Introduction to 4-Benzyloxy-3-methoxyphenol (CAS No. 40232-88-0)
4-Benzyloxy-3-methoxyphenol, identified by its CAS number 40232-88-0, is a significant compound in the field of pharmaceutical chemistry and bioorganic synthesis. This compound, featuring a benzyloxy group and a methoxy substituent on a phenolic ring, has garnered attention due to its versatile structural properties and potential applications in drug development. The unique arrangement of these functional groups makes it a valuable intermediate in the synthesis of more complex molecules, particularly in the creation of bioactive agents.
The< strong>benzyloxy moiety in 4-benzyloxy-3-methoxyphenol contributes to the compound's solubility and stability, which are critical factors in pharmaceutical formulations. This characteristic enhances its utility as a building block in medicinal chemistry. Additionally, the< strong>methoxy group provides a site for further functionalization, enabling chemists to tailor the molecule for specific biological targets. These attributes have positioned 4-benzyloxy-3-methoxyphenol as a compound of interest in both academic research and industrial applications.
In recent years, there has been growing interest in phenolic derivatives due to their demonstrated pharmacological properties. Studies have highlighted the potential of such compounds in addressing various therapeutic challenges, including inflammation, oxidative stress, and infectious diseases. The structural features of 4-benzyloxy-3-methoxyphenol make it a promising candidate for further investigation in these areas. Researchers have been exploring its derivatives to identify novel pharmacophores that could lead to the development of new drugs.
One of the most compelling aspects of 4-benzyloxy-3-methoxyphenol is its role as a precursor in the synthesis of more complex molecules. For instance, it has been utilized in the preparation of flavonoid-like scaffolds, which are known for their broad spectrum of biological activities. The< strong>benzyloxy group can be easily modified through various chemical reactions, such as hydrolysis or coupling reactions, allowing for the introduction of additional functional groups. This flexibility makes it an indispensable tool in synthetic organic chemistry.
The< strong>methoxy group on 4-benzyloxy-3-methoxyphenol also plays a crucial role in its reactivity and functionality. This substituent can participate in electron-deficient aromatic substitution reactions, making it possible to introduce other aromatic or heteroaromatic groups into the molecule. Such modifications can significantly alter the pharmacological profile of the compound, leading to enhanced efficacy or selectivity. These properties have made 4-benzyloxy-3-methoxyphenol a subject of extensive research in medicinal chemistry.
Recent advancements in computational chemistry have further enhanced our understanding of 4-benzyloxy-3-methoxyphenol's behavior. Molecular modeling studies have revealed insights into its interactions with biological targets, providing a rational basis for designing more effective derivatives. These computational approaches have complemented experimental work, allowing researchers to predict and optimize the properties of new compounds derived from 4-benzyloxy-3-methoxyphenol.
The pharmaceutical industry has also recognized the potential of 4-benzyloxy-3-methoxyphenol as an intermediate for drug development. Its structural features make it suitable for use in various drug classes, including anti-inflammatory agents, antioxidants, and antimicrobial compounds. Companies are investing in research to explore new synthetic routes and applications for this compound. The demand for high-quality intermediates like 4-benzyloxy-3-methoxyphenol is expected to grow as pharmaceutical innovation continues to advance.
In conclusion, 4-benzyloxy-3-methoxyphenol (CAS No. 40232-88-0) is a versatile and valuable compound with significant implications in pharmaceutical chemistry and bioorganic synthesis. Its unique structural features and functional groups make it an excellent candidate for further research and development. As our understanding of its properties continues to expand, so too will its applications in creating novel therapeutic agents that address some of today's most pressing medical challenges.
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