Cas no 39250-90-3 (4-methoxy-3,5-dimethylbenzaldehyde)
4-methoxy-3,5-dimethylbenzaldehyde Chemical and Physical Properties
Names and Identifiers
-
- 3,5-Dimethyl-4-methoxybenzaldehyde
- 4-Methoxy-3,5-dimethylbenzaldehyde
- Benzaldehyde,4-methoxy-3,5-dimethyl-
- 4-methoxy-3,5-dimethyl-benzaldehyde
- PubChem2637
- ARONIS023635
- Jsp006819
- SNIGEINPLSDHBQ-UHFFFAOYSA-N
- SBB064672
- 5129AB
- BBL023357
- NE36705
- AS03874
- ST2404643
- BB 0219913
- BENZALDE
- BENZALDEHYDE, 4-METHOXY-3,5-DIMETHYL-
- A824486
- SY029671
- FT-0639538
- CS-W021817
- EN300-53546
- 39250-90-3
- F19844
- SCHEMBL470698
- AKOS005111062
- 3 pound not5-Dimethyl-4-methoxybenzaldehyde
- Z361434506
- MFCD02261755
- DTXSID00374399
- DS-12349
- DB-022093
- 4-methoxy-3,5-dimethylbenzaldehyde
-
- MDL： MFCD02261755
- Inchi： 1S/C10H12O2/c1-7-4-9(6-11)5-8(2)10(7)12-3/h4-6H,1-3H3
- InChI Key： SNIGEINPLSDHBQ-UHFFFAOYSA-N
- SMILES： O(C)C1C(C)=CC(C=O)=CC=1C
Computed Properties
- Exact Mass: 164.08400
- Monoisotopic Mass: 164.084
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
- Complexity: 144
- 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: 26.3
Experimental Properties
- Density: 1.041
- Boiling Point: 264℃ at 760 mmHg
- Flash Point: 112.8°C
- Refractive Index: 1.538
- PSA: 26.30000
- LogP: 2.12450
4-methoxy-3,5-dimethylbenzaldehyde Security Information
-
Hazardous Material Identification：
- HazardClass：IRRITANT
4-methoxy-3,5-dimethylbenzaldehyde Customs Data
- HS CODE：2912499000
- Customs Data：
China Customs Code:
2912499000Overview:
2912499000. Other aldehyde ethers\Aldehydes, phenols and aldehydes containing other oxygen-containing groups. 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, Appearance of tetraformaldehyde
Summary:
2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%
4-methoxy-3,5-dimethylbenzaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | D840136-1g |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 98% | 1g |
313.20 | 2021-05-17 | |
| TRC | D492610-50mg |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 50mg |
$ 50.00 | 2022-06-05 | ||
| TRC | D492610-100mg |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 100mg |
$ 65.00 | 2022-06-05 | ||
| TRC | D492610-500mg |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 500mg |
$ 80.00 | 2022-06-05 | ||
| Fluorochem | 022361-250mg |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 97% | 250mg |
￡17.00 | 2022-03-01 | |
| Fluorochem | 022361-1g |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 97% | 1g |
￡32.00 | 2022-03-01 | |
| Fluorochem | 022361-5g |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 97% | 5g |
￡86.00 | 2022-03-01 | |
| Fluorochem | 022361-10g |
3,5-Dimethyl-4-methoxybenzaldehyde |
39250-90-3 | 97% | 10g |
￡163.00 | 2022-03-01 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 015659-500mg |
4-methoxy-3,5-dimethylbenzaldehyde |
39250-90-3 | 500mg |
519CNY | 2021-05-08 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 015659-1g |
4-methoxy-3,5-dimethylbenzaldehyde |
39250-90-3 | 1g |
795CNY | 2021-05-08 |
4-methoxy-3,5-dimethylbenzaldehyde Suppliers
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Additional information on 4-methoxy-3,5-dimethylbenzaldehyde
4-Methoxy-3,5-Dimethylbenzaldehyde: A Comprehensive Overview
4-Methoxy-3,5-Dimethylbenzaldehyde, also known by its CAS number 39250-90-3, is a versatile aromatic aldehyde with a unique structure that has garnered significant attention in various scientific and industrial fields. This compound is characterized by its benzene ring substituted with a methoxy group at the para position and methyl groups at the meta and para positions relative to the aldehyde functional group. The combination of these substituents imparts distinctive chemical properties, making it a valuable molecule in both academic research and commercial applications.
The synthesis of 4-methoxy-3,5-dimethylbenzaldehyde has been extensively studied, with researchers exploring various methods to optimize its production. Recent advancements have focused on green chemistry approaches, such as using biocatalysts or microwave-assisted synthesis, to enhance yield and reduce environmental impact. These methods not only improve the efficiency of the synthesis process but also align with the growing demand for sustainable chemical manufacturing practices.
In terms of chemical properties, 4-methoxy-3,5-dimethylbenzaldehyde exhibits interesting reactivity due to the electron-donating effects of its substituents. The methoxy group at the para position is known for its strong activating effect, which facilitates electrophilic substitution reactions. This makes the compound a valuable precursor in organic synthesis, particularly in the construction of complex aromatic molecules. Recent studies have demonstrated its utility in synthesizing bioactive compounds, such as potential drug candidates for neurodegenerative diseases.
The application of 4-methoxy-3,5-dimethylbenzaldehyde extends beyond organic synthesis. It has been investigated for its potential in materials science, where it serves as a building block for advanced polymers and materials with tailored properties. For instance, researchers have explored its use in creating stimuli-responsive materials that can change their properties in response to external stimuli like temperature or pH. These materials hold promise for applications in drug delivery systems and smart textiles.
From a pharmacological perspective, 4-methoxy-3,5-dimethylbenzaldehyde has shown intriguing bioactivity. Studies have indicated that it possesses anti-inflammatory and antioxidant properties, making it a potential candidate for therapeutic interventions. Recent research has delved into its mechanism of action, revealing that it interacts with key cellular pathways involved in inflammation and oxidative stress. These findings underscore its potential as a lead compound for drug development.
In conclusion, 4-methoxy-3,5-dimethylbenzaldehyde, CAS number 39250-90-3, is a multifaceted compound with a wide range of applications across various disciplines. Its unique structure and reactivity make it an invaluable tool in organic synthesis, materials science, and pharmacology. As research continues to uncover new insights into its properties and applications, this compound is poised to play an increasingly important role in both academic and industrial settings.
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