Cas no 284040-72-8 (Pyridine, 3-bromo-5-(2-methylpropoxy)-)
Pyridine, 3-bromo-5-(2-methylpropoxy)- Chemical and Physical Properties
Names and Identifiers
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- Pyridine, 3-bromo-5-(2-methylpropoxy)-
- A1-12983
- 284040-72-8
- 3-bromo-5-isobutoxypyridine
- SCHEMBL7102411
- DB-204351
- 3-bromo-5-(2-methylpropoxy)pyridine
- AKOS013526243
-
- MDL: MFCD19674026
- Inchi: 1S/C9H12BrNO/c1-7(2)6-12-9-3-8(10)4-11-5-9/h3-5,7H,6H2,1-2H3
- InChI Key: PQAPXYAYUDZOMS-UHFFFAOYSA-N
- SMILES: BrC1=CN=CC(=C1)OCC(C)C
Computed Properties
- Exact Mass: 229.01023g/mol
- Monoisotopic Mass: 229.01023g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 12
- Rotatable Bond Count: 3
- Complexity: 130
- 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: 2.8
- Topological Polar Surface Area: 22.1?2
Pyridine, 3-bromo-5-(2-methylpropoxy)- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Matrix Scientific | 187085-5g |
3-Bromo-5-(2-methylpropoxy)pyridine, 95% |
284040-72-8 | 95% | 5g |
$1650.00 | 2023-09-07 |
Pyridine, 3-bromo-5-(2-methylpropoxy)- Related Literature
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Bruce Parkinson Energy Environ. Sci., 2010,3, 509-511
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Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
Additional information on Pyridine, 3-bromo-5-(2-methylpropoxy)-
Comprehensive Overview of Pyridine, 3-bromo-5-(2-methylpropoxy)- (CAS No. 284040-72-8)
Pyridine, 3-bromo-5-(2-methylpropoxy)- (CAS No. 284040-72-8) is a specialized organic compound that has garnered significant attention in recent years due to its unique structural properties and potential applications in pharmaceutical and agrochemical research. This brominated pyridine derivative, characterized by its 3-bromo-5-(2-methylpropoxy) substitution pattern, serves as a versatile intermediate in synthetic chemistry. Its molecular formula, C9H12BrNO, and distinct functional groups make it a valuable building block for designing novel compounds with tailored biological activities.
The growing interest in pyridine derivatives stems from their prevalence in drug discovery and material science. Researchers frequently search for "3-bromo-5-(2-methylpropoxy)pyridine synthesis" or "CAS 284040-72-8 applications," reflecting the compound's relevance in modern chemistry. Recent advancements in heterocyclic chemistry have highlighted the importance of such brominated pyridines as precursors for cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig reactions, which are pivotal in creating complex molecular architectures.
From an industrial perspective, Pyridine, 3-bromo-5-(2-methylpropoxy)- is often discussed alongside "high-value chemical intermediates" and "custom synthesis solutions." Its stability under various reaction conditions and compatibility with diverse catalysts make it a preferred choice for pharmaceutical manufacturers exploring "targeted drug delivery systems" and "small molecule therapeutics." The compound's 2-methylpropoxy side chain further enhances its lipophilicity, a property increasingly sought after in the development of CNS-active compounds.
Environmental and regulatory considerations have also shaped discussions around 284040-72-8. With the chemical industry moving toward "green chemistry principles," researchers are investigating sustainable methods for producing this intermediate. Queries like "eco-friendly bromination techniques" and "catalytic alternatives for pyridine functionalization" demonstrate the evolving priorities in synthetic methodology. The compound's role in "biodegradable agrochemicals" research further aligns with global sustainability trends.
Analytical characterization of Pyridine, 3-bromo-5-(2-methylpropoxy)- typically involves advanced techniques such as HPLC, GC-MS, and NMR spectroscopy. Quality control specifications for CAS 284040-72-8 often include parameters like purity (>98%), residual solvent content, and heavy metal limits, reflecting its pharmaceutical-grade applications. These standards address common purchaser concerns about "chemical purity verification" and "batch-to-batch consistency."
Market trends indicate rising demand for functionalized pyridines like 3-bromo-5-(2-methylpropoxy)pyridine, particularly in Asia-Pacific research hubs. This growth parallels increased investment in "precision medicine" and "agrochemical innovation." The compound's patent landscape reveals ongoing research into its derivatives, with particular interest in their potential as "kinase inhibitors" and "allosteric modulators" - two hot topics in current medicinal chemistry literature.
Storage and handling recommendations for 284040-72-8 emphasize standard organic compound protocols: protection from moisture, storage at controlled temperatures, and use in well-ventilated areas. These guidelines address frequently searched terms like "chemical storage best practices" while ensuring compliance with international laboratory safety standards. The compound's stability profile makes it suitable for global distribution, contributing to its accessibility for research institutions worldwide.
Future research directions for Pyridine, 3-bromo-5-(2-methylpropoxy)- may explore its incorporation into "metal-organic frameworks" (MOFs) or as a ligand in catalytic systems. The intersection of "computational chemistry" and "materials science" opens new possibilities for predicting and optimizing its properties. As synthetic methodologies advance, this compound will likely maintain its status as a valuable tool for chemists addressing challenges in "molecular diversity" and "structure-activity relationships."
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