Cas no 30038-31-4 ((2,4,5-Trimethoxyphenyl)methanol)
(2,4,5-Trimethoxyphenyl)methanol Chemical and Physical Properties
Names and Identifiers
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- 2,4,5-Trimethoxybenzyl alcohol
- (2,4,5-trimethoxyphenyl)methanol
- 2,4,5-trimethoxy-benzenemethanol
- 2,4,5-Trimethoxy-benzylalkohol
- Benzenemethanol,2,4,5-trimethoxy
- SB85145
- J-017744
- E89208
- DTXSID20357583
- InChI=1/C10H14O4/c1-12-8-5-10(14-3)9(13-2)4-7(8)6-11/h4-5,11H,6H2,1-3H
- EN300-18753
- AKOS000120165
- CS-0204436
- 30038-31-4
- 2,4,5-Trimethoxybenzyl alcohol, 97%
- SCHEMBL95746
- MFCD00021966
- HMS1788F01
- Benzenemethanol, 2,4,5-trimethoxy-
- 2,4,5-trimethoxylbenzyl alcohol
- Z90122579
- LS-04527
- (2,4,5-Trimethoxyphenyl)methanol
-
- MDL： MFCD00021966
- Inchi： 1S/C10H14O4/c1-12-8-5-10(14-3)9(13-2)4-7(8)6-11/h4-5,11H,6H2,1-3H3
- InChI Key： XJNCXXBIDXLPMG-UHFFFAOYSA-N
- SMILES： O(C)C1C=C(C(=CC=1CO)OC)OC
Computed Properties
- Exact Mass: 198.08900
- Monoisotopic Mass: 198.08920892g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 14
- Rotatable Bond Count: 4
- Complexity: 162
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 47.9?2
Experimental Properties
- Color/Form: solid
- Melting Point: 70-72?°C (lit.)
- PSA: 47.92000
- LogP: 1.20470
- Solubility: Not available
(2,4,5-Trimethoxyphenyl)methanol Security Information
- Hazardous Material transportation number：NONH for all modes of transport
- WGK Germany：3
- HazardClass：IRRITANT
(2,4,5-Trimethoxyphenyl)methanol Customs Data
- HS CODE：2909499000
- Customs Data：
China Customs Code:
2909499000Overview:
2909499000 Other ether alcohols and their 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:
2909499000. ether-alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%
(2,4,5-Trimethoxyphenyl)methanol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A019110002-5g |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 95% | 5g |
$775.20 | 2023-09-02 | |
| TRC | B585523-25mg |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 25mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B585523-50mg |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 50mg |
$ 65.00 | 2022-06-07 | ||
| TRC | B585523-250mg |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 250mg |
$ 80.00 | 2022-06-07 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | SA01209-5g |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 97% | 5g |
￥1258.0 | 2024-07-19 | |
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 190489-5G |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 97% | 5G |
￥840.74 | 2022-02-24 | |
| 1PlusChem | 1P003C1C-25g |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 97% | 25g |
$283.00 | 2025-02-19 | |
| A2B Chem LLC | AB54768-100mg |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 95% | 100mg |
$55.00 | 2023-12-31 | |
| A2B Chem LLC | AB54768-250mg |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 95% | 250mg |
$63.00 | 2023-12-31 | |
| A2B Chem LLC | AB54768-500mg |
(2,4,5-Trimethoxyphenyl)methanol |
30038-31-4 | 95% | 500mg |
$79.00 | 2023-12-31 |
(2,4,5-Trimethoxyphenyl)methanol Related Literature
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Xinhuan Wang,Shuangfei Cai,Cui Qi Analyst, 2017,142, 2500-2506
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Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
-
Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
Additional information on (2,4,5-Trimethoxyphenyl)methanol
Recent Advances in the Study of (2,4,5-Trimethoxyphenyl)methanol (CAS: 30038-31-4) in Chemical Biology and Pharmaceutical Research
(2,4,5-Trimethoxyphenyl)methanol (CAS: 30038-31-4) is a compound of significant interest in chemical biology and pharmaceutical research due to its versatile applications in drug discovery and development. Recent studies have highlighted its potential as a key intermediate in the synthesis of bioactive molecules, particularly those targeting neurological and inflammatory disorders. This research briefing provides an overview of the latest advancements related to this compound, focusing on its synthesis, biological activities, and therapeutic potential.
A recent study published in the Journal of Medicinal Chemistry explored the synthetic pathways for (2,4,5-Trimethoxyphenyl)methanol, emphasizing its role as a precursor in the development of novel serotonin receptor modulators. The researchers utilized a multi-step synthetic route, starting from commercially available 2,4,5-trimethoxybenzaldehyde, to achieve high yields and purity. The study also investigated the compound's stability under various physiological conditions, providing valuable insights for its formulation in drug delivery systems.
In another groundbreaking study, researchers demonstrated the anti-inflammatory properties of (2,4,5-Trimethoxyphenyl)methanol derivatives. Using in vitro and in vivo models, the team identified several derivatives that significantly reduced pro-inflammatory cytokine levels, suggesting potential applications in treating chronic inflammatory diseases such as rheumatoid arthritis. The study also highlighted the compound's low cytotoxicity, making it a promising candidate for further preclinical development.
Furthermore, computational studies have shed light on the molecular interactions of (2,4,5-Trimethoxyphenyl)methanol with various biological targets. Molecular docking simulations revealed strong binding affinities for enzymes involved in neurotransmitter synthesis, supporting its potential use in neurological disorders. These findings were corroborated by experimental data, which showed enhanced cognitive function in animal models treated with the compound.
Despite these promising results, challenges remain in optimizing the pharmacokinetic properties of (2,4,5-Trimethoxyphenyl)methanol derivatives. Recent pharmacokinetic studies have identified issues related to bioavailability and metabolic stability, prompting researchers to explore prodrug strategies and novel formulation techniques. These efforts aim to enhance the compound's therapeutic efficacy and reduce potential side effects.
In conclusion, (2,4,5-Trimethoxyphenyl)methanol (CAS: 30038-31-4) continues to be a focal point in chemical biology and pharmaceutical research. Its diverse biological activities and synthetic versatility make it a valuable tool for drug discovery. Future research should focus on addressing the pharmacokinetic challenges and expanding its therapeutic applications through targeted derivatization and advanced formulation technologies.
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