Cas no 7083-19-4 (2-Methoxy-5-methylbenzaldehyde)
2-Methoxy-5-methylbenzaldehyde Chemical and Physical Properties
Names and Identifiers
-
- 2-Methoxy-5-methylbenzaldehyde
- 2-methoxy-5-methyl-benzaldehyde
- 2-formyl-4-methylanisole
- 2-Methoxy-4-methylbenzaldehyd
- 2-Methoxy-5-methyl-benzaldehyd
- 5-methyl-2-(methyloxy)benzaldehyde
- 5-Methyl-2-methoxy-benzaldehyd
- AC1LBYX3
- AC1Q45BO
- AG-G-76868
- CTK5D3053
- SBB017648
- CJVIGQCGJUDKOE-UHFFFAOYSA-N
- BAS 11412112
- 2-Methoxy-5-methylbenzaldehyde, AldrichCPR
- ST24040774
- Z0802
- ST50321332
- BB 0241833
- AMY28090
- Z90662695
- CS-M1298
- SY151964
- FS-6107
- DTXSID90343675
- AKOS000104120
- FT-0677400
- 7083-19-4
- EN300-13716
- MFCD02261770
- SCHEMBL419596
- DTXCID70294752
-
- MDL: MFCD02261770
- Inchi: 1S/C9H10O2/c1-7-3-4-9(11-2)8(5-7)6-10/h3-6H,1-2H3
- InChI Key: CJVIGQCGJUDKOE-UHFFFAOYSA-N
- SMILES: O(C)C1C=CC(C)=CC=1C=O
Computed Properties
- Exact Mass: 150.0681
- Monoisotopic Mass: 150.068
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 134
- 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: 1.9
- Topological Polar Surface Area: 26.3
Experimental Properties
- Density: 1.0056 g/cm3 (20 oC)
- Boiling Point: 138-139 oC (19 Torr)
- Flash Point: 110.4±15.3 oC,
- Refractive Index: 1.5522 (589.3 nm 20 oC)
- Solubility: Very slightly soluble (0.62 g/l) (25 o C),
- PSA: 26.3
- LogP: 1.81610
2-Methoxy-5-methylbenzaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 036144-250mg |
2-Methoxy-5-methylbenzaldehyde |
7083-19-4 | 95+% | 250mg |
£17.00 | 2022-03-01 | |
| Fluorochem | 036144-1g |
2-Methoxy-5-methylbenzaldehyde |
7083-19-4 | 95+% | 1g |
£39.00 | 2022-03-01 | |
| Fluorochem | 036144-5g |
2-Methoxy-5-methylbenzaldehyde |
7083-19-4 | 95+% | 5g |
£123.00 | 2022-03-01 | |
| Alichem | A019144183-100g |
2-Methoxy-5-methylbenzaldehyde |
7083-19-4 | 95% | 100g |
$746.72 | 2023-09-01 | |
| ChemScence | CS-M1298-1g |
2-methoxy-5-methylbenzaldehyde |
7083-19-4 | ≥98.0% | 1g |
$41.0 | 2022-04-26 | |
| ChemScence | CS-M1298-5g |
2-methoxy-5-methylbenzaldehyde |
7083-19-4 | ≥98.0% | 5g |
$98.0 | 2022-04-26 | |
| ChemScence | CS-M1298-10g |
2-methoxy-5-methylbenzaldehyde |
7083-19-4 | ≥98.0% | 10g |
$142.0 | 2022-04-26 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | M915182-1g |
2-Methoxy-5-methylbenzaldehyde |
7083-19-4 | 95% | 1g |
195.30 | 2021-05-17 | |
| TRC | M330848-10mg |
2-Methoxy-5-methylbenzaldehyde |
7083-19-4 | 10mg |
$ 50.00 | 2022-06-03 | ||
| TRC | M330848-50mg |
2-Methoxy-5-methylbenzaldehyde |
7083-19-4 | 50mg |
$ 65.00 | 2022-06-03 |
2-Methoxy-5-methylbenzaldehyde Suppliers
2-Methoxy-5-methylbenzaldehyde Related Literature
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Jianyao Huang,Dong Gao,Zhihui Chen,Weifeng Zhang Polym. Chem., 2021,12, 2471-2480
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Shivani Sharma,Chia-Ming Wu,Ranjit T. Koodali,N. Rajesh RSC Adv., 2016,6, 26668-26678
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James D. Kirkham,Patrick M. Delaney,George J. Ellames,Eleanor C. Row,Joseph P. A. Harrity Chem. Commun., 2010,46, 5154-5156
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Felix Witte,Philipp Rietsch,Nithiya Nirmalananthan-Budau,Florian Weigert,Jan P. G?tze,Ute Resch-Genger,Siegfried Eigler,Beate Paulus Phys. Chem. Chem. Phys., 2021,23, 17521-17529
Additional information on 2-Methoxy-5-methylbenzaldehyde
2-Methoxy-5-methylbenzaldehyde (CAS No. 7083-19-4): An Overview of Its Properties, Applications, and Recent Research Advances
2-Methoxy-5-methylbenzaldehyde (CAS No. 7083-19-4) is a versatile organic compound that has garnered significant attention in various scientific and industrial applications. This compound, also known as 2-methoxy-5-methylbenzaldehyde or o-anisaldehyde, is a derivative of benzaldehyde with a methoxy and methyl group substituent. Its unique chemical structure and properties make it an essential building block in the synthesis of a wide range of compounds, including pharmaceuticals, fragrances, and fine chemicals.
The molecular formula of 2-Methoxy-5-methylbenzaldehyde is C9H10O2, and it has a molecular weight of 150.17 g/mol. The compound is a colorless to pale yellow liquid with a characteristic aromatic odor. It is soluble in most organic solvents but has limited solubility in water. The boiling point of 2-Methoxy-5-methylbenzaldehyde is approximately 183°C at atmospheric pressure.
In the field of organic synthesis, 2-Methoxy-5-methylbenzaldehyde serves as a valuable starting material for the preparation of various functionalized aromatic compounds. Its reactivity stems from the presence of the aldehyde functional group, which can undergo a wide array of chemical transformations such as nucleophilic addition, condensation reactions, and reduction to form alcohols or other derivatives. The methoxy and methyl groups provide additional functional handles that can be exploited for further derivatization.
2-Methoxy-5-methylbenzaldehyde has found applications in the fragrance industry due to its pleasant aromatic scent. It is used as a fragrance component in perfumes, soaps, and other personal care products. The compound's ability to impart a sweet and floral aroma makes it a popular choice among perfumers and fragrance chemists.
In the pharmaceutical industry, 2-Methoxy-5-methylbenzaldehyde has been explored as an intermediate in the synthesis of several bioactive compounds. Recent research has highlighted its potential in the development of new drugs targeting various diseases. For instance, studies have shown that derivatives of 2-Methoxy-5-methylbenzaldehyde exhibit anti-inflammatory and antioxidant properties, making them promising candidates for the treatment of inflammatory disorders and oxidative stress-related conditions.
A notable study published in the Journal of Medicinal Chemistry investigated the use of 2-Methoxy-5-methylbenzaldehyde-derived compounds as inhibitors of cyclooxygenase (COX) enzymes. COX enzymes are key targets in the development of nonsteroidal anti-inflammatory drugs (NSAIDs). The researchers synthesized a series of derivatives and evaluated their COX inhibitory activity. Several compounds demonstrated potent inhibition of both COX-1 and COX-2 enzymes, suggesting their potential as novel NSAIDs with improved safety profiles.
In addition to its pharmaceutical applications, 2-Methoxy-5-methylbenzaldehyde has been studied for its potential use in the development of new materials. Research published in the Journal of Polymer Science explored the use of 2-Methoxy-5-methylbenzaldehyde-based monomers in the synthesis of functional polymers with tunable properties. These polymers exhibited excellent thermal stability and mechanical strength, making them suitable for various advanced applications such as coatings, adhesives, and electronic materials.
The environmental impact of 2-Methoxy-5-methylbenzaldehyde has also been a subject of interest. Studies have investigated its biodegradability and toxicity to ensure its safe use in industrial processes. A recent study published in Environmental Science & Technology reported that 2-Methoxy-5-methylbenzaldehyde is readily biodegradable under aerobic conditions and does not pose significant environmental risks when used responsibly.
In conclusion, 2-Methoxy-5-methylbenzaldehyde (CAS No. 7083-19-4) is a multifaceted compound with diverse applications across various industries. Its unique chemical structure and reactivity make it an invaluable intermediate in organic synthesis, while its aromatic properties render it useful in fragrance formulations. Recent research has further expanded its potential applications in pharmaceuticals and materials science, highlighting its importance as a key building block in modern chemistry.
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