Cas no 109346-81-8 (Benzeneacetaldehyde, 3-chloro-4-methyl-)
Benzeneacetaldehyde, 3-chloro-4-methyl- Chemical and Physical Properties
Names and Identifiers
-
- Benzeneacetaldehyde, 3-chloro-4-methyl-
- 2-(3-Chloro-4-methylphenyl)acetaldehyde
- A1-42409
- 109346-81-8
- SCHEMBL7044076
- AKOS006324557
- CS-0350305
- EN300-1985657
-
- Inchi: 1S/C9H9ClO/c1-7-2-3-8(4-5-11)6-9(7)10/h2-3,5-6H,4H2,1H3
- InChI Key: WOGRNQUBKPXKSE-UHFFFAOYSA-N
- SMILES: ClC1C=C(C=CC=1C)CC=O
Computed Properties
- Exact Mass: 168.0341926g/mol
- Monoisotopic Mass: 168.0341926g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 136
- 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: 2.3
- Topological Polar Surface Area: 17.1?2
Benzeneacetaldehyde, 3-chloro-4-methyl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1985657-0.05g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 0.05g |
$912.0 | 2023-05-31 | ||
| Enamine | EN300-1985657-0.1g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 0.1g |
$956.0 | 2023-05-31 | ||
| Enamine | EN300-1985657-0.25g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 0.25g |
$999.0 | 2023-05-31 | ||
| Enamine | EN300-1985657-0.5g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 0.5g |
$1043.0 | 2023-05-31 | ||
| Enamine | EN300-1985657-1.0g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 1g |
$1086.0 | 2023-05-31 | ||
| Enamine | EN300-1985657-2.5g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 2.5g |
$2127.0 | 2023-05-31 | ||
| Enamine | EN300-1985657-5.0g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 5g |
$3147.0 | 2023-05-31 | ||
| Enamine | EN300-1985657-10.0g |
2-(3-chloro-4-methylphenyl)acetaldehyde |
109346-81-8 | 10g |
$4667.0 | 2023-05-31 |
Benzeneacetaldehyde, 3-chloro-4-methyl- Related Literature
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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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
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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4. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
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Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
Additional information on Benzeneacetaldehyde, 3-chloro-4-methyl-
Exploring Benzeneacetaldehyde, 3-chloro-4-methyl- (CAS No. 109346-81-8): Properties, Applications, and Market Insights
Benzeneacetaldehyde, 3-chloro-4-methyl- (CAS No. 109346-81-8) is a specialized organic compound that has garnered attention in various industrial and research applications. This aromatic aldehyde derivative is characterized by its unique molecular structure, featuring a chloro and methyl substitution on the benzene ring. Its chemical formula, C9H9ClO, and molecular weight of 168.62 g/mol make it a versatile intermediate in synthetic chemistry. Researchers and manufacturers value this compound for its role in producing fragrances, pharmaceuticals, and agrochemicals.
The growing demand for 3-chloro-4-methylbenzeneacetaldehyde is driven by its utility in creating high-value derivatives. For instance, it serves as a precursor in the synthesis of flavor and fragrance compounds, which are increasingly sought after in the food and cosmetics industries. With consumers leaning toward natural and sustainable products, the compound's role in developing bio-based aroma chemicals has become a hot topic. Additionally, its application in pharmaceutical intermediates aligns with the booming healthcare sector, particularly in the development of novel therapeutic agents.
From a chemical perspective, Benzeneacetaldehyde, 3-chloro-4-methyl- exhibits notable stability under standard conditions, making it suitable for storage and transportation. Its boiling point and melting point data are critical for industrial processes, ensuring optimal reaction conditions. Analytical techniques such as GC-MS and HPLC are commonly employed to verify its purity, which is essential for end-use applications. The compound's solubility in organic solvents like ethanol and acetone further enhances its versatility in synthetic pathways.
In the context of market trends, the demand for chlorinated aromatic aldehydes like 109346-81-8 is on the rise. The Asia-Pacific region, in particular, has seen significant growth due to expanding chemical and pharmaceutical industries. Environmental regulations and the push for green chemistry have also influenced production methods, with manufacturers adopting cleaner and more efficient synthesis routes. This shift not only meets regulatory standards but also appeals to eco-conscious buyers.
Another area of interest is the compound's potential in material science. Recent studies explore its use in polymer modification and specialty coatings, where its aromatic and reactive aldehyde group can enhance material properties. Innovations in smart materials and nanotechnology have opened new avenues for 3-chloro-4-methylbenzeneacetaldehyde, positioning it as a valuable asset in advanced manufacturing.
For researchers and procurement specialists, understanding the supply chain dynamics of Benzeneacetaldehyde, 3-chloro-4-methyl- is crucial. Factors like raw material availability, production capacity, and geopolitical influences can impact pricing and lead times. Companies are increasingly leveraging digital platforms and AI-driven analytics to optimize sourcing strategies, ensuring a steady supply of this high-demand chemical.
In summary, Benzeneacetaldehyde, 3-chloro-4-methyl- (CAS No. 109346-81-8) is a multifaceted compound with broad applications across industries. Its role in fragrance synthesis, pharmaceutical development, and advanced materials underscores its importance in modern chemistry. As market demands evolve and technological advancements continue, this compound is poised to remain a key player in the specialty chemicals sector.
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