Cas no 1427396-66-4 (4-chloro-2-hydroxy-6-methoxybenzaldehyde)
4-chloro-2-hydroxy-6-methoxybenzaldehyde Chemical and Physical Properties
Names and Identifiers
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- 4-chloro-2-hydroxy-6-methoxyBenzaldehyde
- Benzaldehyde, 4-chloro-2-hydroxy-6-methoxy-
- SUWIKBDAVNNQSD-UHFFFAOYSA-N
- CID 86700905
- 4-chloro-2-hydroxy-6-methoxybenzaldehyde
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- Inchi: 1S/C8H7ClO3/c1-12-8-3-5(9)2-7(11)6(8)4-10/h2-4,11H,1H3
- InChI Key: SUWIKBDAVNNQSD-UHFFFAOYSA-N
- SMILES: ClC1C=C(C(C=O)=C(C=1)OC)O
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
- Complexity: 162
- Topological Polar Surface Area: 46.5
Experimental Properties
- Density: 1.377±0.06 g/cm3(Predicted)
- Boiling Point: 294.4±35.0 °C(Predicted)
- pka: 6.83±0.15(Predicted)
4-chloro-2-hydroxy-6-methoxybenzaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| A2B Chem LLC | AE64795-100mg |
4-Chloro-2-hydroxy-6-methoxybenzaldehyde |
1427396-66-4 | 96% | 100mg |
$532.00 | 2024-04-20 | |
| A2B Chem LLC | AE64795-250mg |
4-Chloro-2-hydroxy-6-methoxybenzaldehyde |
1427396-66-4 | 96% | 250mg |
$1054.00 | 2024-04-20 |
4-chloro-2-hydroxy-6-methoxybenzaldehyde Related Literature
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
Additional information on 4-chloro-2-hydroxy-6-methoxybenzaldehyde
Comprehensive Analysis of 4-Chloro-2-hydroxy-6-methoxybenzaldehyde (CAS No. 1427396-66-4): Properties, Applications, and Industry Trends
4-Chloro-2-hydroxy-6-methoxybenzaldehyde (CAS 1427396-66-4) is a specialized aromatic aldehyde compound gaining attention in pharmaceutical and agrochemical research. This chlorinated benzaldehyde derivative features a unique molecular structure with methoxy and hydroxy functional groups, making it valuable for synthesizing complex organic molecules. Recent studies highlight its potential as a key intermediate in developing novel bioactive compounds, particularly in antimicrobial and antioxidant applications.
The compound's structural characteristics—including its electron-withdrawing chloro group and electron-donating methoxy group—create interesting reactivity patterns. Researchers are exploring its use in green chemistry applications, aligning with the growing demand for sustainable synthesis methods. Analytical techniques like HPLC and NMR spectroscopy confirm its high purity (>98%), a critical factor for precision applications in drug discovery programs.
Market trends show increasing searches for "4-chloro-2-hydroxy-6-methoxybenzaldehyde suppliers" and "CAS 1427396-66-4 technical specifications," reflecting industrial interest. The compound's low environmental persistence compared to similar halogenated aromatics makes it attractive for eco-friendly formulations. Its melting point (128-131°C) and solubility profile enable diverse organic synthesis applications, from flavor/fragrance precursors to photostabilizers in polymer chemistry.
Recent patent filings reveal innovative uses in crop protection formulations, addressing the agricultural sector's need for next-generation pesticides with reduced ecological impact. The compound's hydrogen-bonding capacity facilitates molecular recognition processes, making it valuable for supramolecular chemistry applications. Quality-conscious buyers frequently search for "4-chloro-2-hydroxy-6-methoxybenzaldehyde HPLC purity" and "1427396-66-4 stability data," emphasizing the importance of rigorous characterization.
In pharmaceutical contexts, the compound serves as a versatile building block for heterocyclic synthesis, particularly in developing chiral auxiliaries and asymmetric catalysts. Its limited toxicity profile (as per preliminary studies) positions it favorably against traditional halogenated intermediates. The rise of AI-assisted molecular design has increased demand for well-characterized compounds like this, as evidenced by search trends for "benzaldehyde derivatives for machine learning" in chemical databases.
Storage recommendations typically suggest amber glass containers under inert atmosphere to maintain stability, with particular attention to moisture sensitivity. Analytical reference standards of this compound are becoming essential for quality control laboratories, especially in regions with strict ICH guidelines compliance requirements. The compound's UV absorption properties around 280 nm make it suitable for certain photocatalytic applications currently under investigation.
Manufacturing processes have evolved to incorporate continuous flow chemistry methods, improving yield and reducing waste—a response to growing "green chemistry" queries in search engines. The compound's crystalline form shows excellent batch-to-batch reproducibility, crucial for regulatory submissions in pharmaceutical applications. Recent publications explore its potential in metal-organic frameworks (MOFs), tapping into the booming materials science research sector.
Global regulatory status varies, with most markets classifying it as a non-hazardous chemical under normal handling conditions. This status, combined with its synthetic utility, explains rising searches for "1427396-66-4 global availability" among contract research organizations. The compound's structural motif appears in several natural product analogs, driving interest from medicinal chemistry teams working on bioinspired compounds.
Future research directions may explore its electrochemical properties for energy storage applications, given the growing focus on renewable energy technologies. The compound's cost-effectiveness compared to similar multifunctional aldehydes makes it attractive for industrial-scale applications. As analytical techniques advance, particularly in cryo-EM and microED, the demand for precisely characterized small molecules like this will likely increase.
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