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3-BROMO-2-ETHOXYPYRIDINE CAS:57883-25-7
3-Bromo-2-ethoxypyridine is an organic compound featuring a pyridine ring with bromine and ethoxy substituents at specific positions. Its molecular formula is C9H10BrN, making it an important intermediate in organic synthesis. The presence of the bromine atom enhances the compound’s reactivity, allowing for various chemical transformations, including nucleophilic substitutions and coupling reactions. It is often utilized in the development of pharmaceuticals and agrochemicals due to its diverse biological activities. Understanding the properties and reactivity of 3-bromo-2-ethoxypyridine can facilitate the design of novel compounds with potential therapeutic applications.
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2-Chloro-3-bromo-5-aminopyridine CAS:130284-53-6
2-Chloro-3-bromo-5-aminopyridine is an organic compound characterized by the molecular formula C5H4BrClN2. It features a pyridine ring with a chlorine atom at the 2-position, a bromine atom at the 3-position, and an amino group at the 5-position. The specific arrangement of these substituents imparts unique electronic properties to the compound, making it a valuable intermediate in synthetic chemistry. Its structure allows for various chemical transformations, including nucleophilic substitutions and coupling reactions, which are crucial in pharmaceutical and agrochemical development. This compound is significant in research aimed at discovering new bioactive molecules and advanced materials.
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2-CHLORO-3-FLUORO-4-FORMYLPYRIDINE CAS:329794-28-7
2-Chloro-3-fluoro-4-formylpyridine is an organic compound with the molecular formula C6H4ClFNO. It features a pyridine ring substituted with a chlorine atom at the 2-position, a fluorine atom at the 3-position, and a formyl group (-CHO) at the 4-position. This unique substitution pattern imparts distinct electronic properties that enhance its reactivity. The presence of halogens increases electrophilicity, making it suitable for nucleophilic substitutions and other chemical transformations. Commonly utilized in medicinal chemistry, 2-chloro-3-fluoro-4-formylpyridine serves as a valuable intermediate for synthesizing various bioactive compounds and new pharmaceuticals.
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3-Iodopyridin-2-amine CAS:104830-06-0
3-Iodopyridin-2-amine is an organic compound characterized by the molecular formula C5H5IN2. This molecule features a pyridine ring with an iodide substituent at the 3-position and an amino group at the 2-position. The presence of iodine introduces significant electrophilic character, while the amino group enhances nucleophilicity, resulting in unique chemical reactivity. As a versatile intermediate, 3-iodopyridin-2-amine plays a crucial role in organic synthesis, particularly in the pharmaceutical industry, where it can be used to develop various bioactive compounds. Its distinctive structure also makes it relevant in materials science for the design of functionalized materials.
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3-Amino-2-picoline CAS:3430-10-2
3-Amino-2-picoline is an organic compound with the molecular formula C6H8N2. It consists of a pyridine ring with an amino group at the 3-position and a methyl group at the 2-position. This unique substitution pattern influences its chemical properties, making it a valuable intermediate in organic synthesis. The amino group imparts nucleophilic character, while the presence of the methyl group can affect electronic distribution, enhancing the compound’s reactivity. 3-Amino-2-picoline finds applications in pharmaceuticals, agrochemicals, and materials science, where it serves as a building block for developing bioactive compounds and functional materials.
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2-CHLORO-5-FLUORO-3-HYDROXYPYRIDINE CAS:884494-35-3
2-Chloro-5-fluoro-3-hydroxypyridine is an organic compound with the molecular formula C6H5ClFNO. It features a pyridine ring substituted with a chlorine atom at the 2-position, a fluorine atom at the 5-position, and a hydroxyl group (-OH) at the 3-position. This unique substitution pattern affects its electronic properties, enhancing reactivity and making it suitable for various chemical transformations. The presence of halogens increases electrophilicity, while the hydroxyl group allows for hydrogen bonding interactions. Commonly employed in medicinal chemistry, 2-chloro-5-fluoro-3-hydroxypyridine acts as an important intermediate for synthesizing diverse bioactive compounds.
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3-Amino-5-bromo-2-chloropyridine CAS:588729-99-1
3-Amino-5-bromo-2-chloropyridine is an organic compound with the molecular formula C5H4BrClN2. It features a pyridine ring substituted with an amino group at the 3-position, a bromo group at the 5-position, and a chloro group at the 2-position. This unique substitution pattern endows the compound with distinct electronic properties, making it a valuable intermediate in synthetic chemistry. The presence of both electron-withdrawing (bromo and chloro) and electron-donating (amino) groups influences its reactivity in various chemical reactions, particularly in drug discovery and agrochemical development, highlighting its significance in both medicinal and organic chemistry research.
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3,5-DICHLOROISONICOTINIC ACID CAS:13958-93-5
3,5-Dichoroisonicotinic acid is an organic compound with the molecular formula C6H3Cl2N O2. It consists of a pyridine ring with carboxylic acid functionality, featuring two chlorine substituents at the 3- and 5- positions. This compound is significant in organic synthesis and medicinal chemistry, serving as an important intermediate for developing various pharmaceuticals and agrochemicals. The presence of dichlorination enhances its reactivity, allowing it to participate in diverse chemical reactions. Research into 3,5-dichloroisonicotinic acid can lead to new compounds with potential therapeutic applications, making it a subject of interest for both chemists and pharmacologists.
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2-Chloro-4-methyl-3-nitropyridine CAS:23056-39-5
2-Chloro-4-methyl-3-nitropyridine is an organic compound with the molecular formula C6H6ClN O2. It consists of a pyridine ring that features a chlorine atom at the 2-position, a methyl group at the 4-position, and a nitro group at the 3-position. This unique substitution pattern confers distinctive electronic properties, making it a valuable intermediate in synthetic chemistry. The presence of both electron-donating (methyl) and electron-withdrawing (nitro, chloro) substituents influences its reactivity, allowing for diverse chemical transformations. Research into this compound has potential applications in pharmaceuticals and agrochemicals, highlighting its significance in medicinal chemistry.
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5-ACETYL-2-METHOXYPYRIDINE, 97% CAS:213193-32-9
5-Acetyl-2-methoxypyridine is an organic compound with the molecular formula C8H9NO2. It features a pyridine ring substituted with an acetyl group at the 5-position and a methoxy group at the 2-position. This molecule exhibits interesting electronic characteristics due to the presence of both electron-donating (methoxy) and electron-withdrawing (acetyl) groups, influencing its reactivity in various chemical processes. The compound holds significance in organic synthesis, particularly as a building block for pharmaceuticals and agrochemicals. Its versatile reactivity enables diverse transformations, making it a valuable intermediate in synthetic chemistry and research into new biologically active compounds.
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2-BROMO-4,6-DIMETHYLPYRIDINE CAS:4926-26-5
2-Bromo-4,6-dimethylpyridine is an organic compound with the molecular formula C8H10BrN. It features a pyridine ring that is substituted with a bromine atom at the 2-position and two methyl groups at the 4- and 6-positions. This unique substitution pattern enhances the molecule’s electronic properties, making it a valuable intermediate in organic synthesis. The presence of the bromine atom facilitates nucleophilic substitutions, while the methyl groups affect sterics and reactivity. Commonly used in pharmaceuticals and agrochemicals, 2-bromo-4,6-dimethylpyridine serves as a precursor for various bioactive compounds and functional materials.
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2,4-Dibromonicotinic acid CAS:1269291-41-9
2,4-Dibromonicotinic acid is an organic compound with the molecular formula C6H4Br2N O2. It features a pyridine ring with bromine substituents at the 2- and 4- positions and a carboxylic acid functional group. This compound is of interest in organic synthesis and medicinal chemistry as it serves as an important intermediate in the preparation of various pharmaceuticals and agrochemicals. The presence of bromine enhances its reactivity, allowing for versatile chemical transformations. Investigating the properties and behavior of 2,4-dibromonicotinic acid can lead to the development of new compounds with potential therapeutic applications.
