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5-Iodosalicylic acid CAS:119-30-2
5-Iodosalicylic acid is a halogenated derivative of salicylic acid, distinguished by the presence of an iodine atom at the 5-position of the aromatic ring. As a member of the salicylate family, this compound exhibits significant biological and pharmacological activities, including anti-inflammatory, antimicrobial, and analgesic properties. The introduction of the iodine atom enhances its reactivity and opens pathways for further chemical modifications, making it a useful intermediate in organic synthesis. 5-Iodosalicylic acid has potential applications in pharmaceutical development and research, particularly in the design of new therapeutic agents targeting various diseases.
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4-Iodobenzonitrile CAS:3058-39-7
4-Iodobenzonitrile is an organic compound characterized by a cyano group (-CN) and an iodine atom attached to a benzene ring at the para position. This compound, with the molecular formula C7H4BrN, belongs to the class of halogenated aromatic compounds and exhibits unique chemical properties due to the presence of both the halogen and nitrile functional groups. The iodine atom enhances the compound’s reactivity, making it useful in various synthetic applications, including organic synthesis and materials science. 4-Iodobenzonitrile serves as an important building block in pharmaceuticals, agrochemicals, and other fine chemicals, highlighting its versatility in different chemical contexts.
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Methyl 4-iodobenzoate CAS:619-44-3
Methyl 4-iodobenzoate is an organic compound belonging to the class of aryl halides. It features a methyl ester group attached to a benzoate ring, with an iodine atom positioned at the para position relative to the ester functional group. This compound is known for its diverse applications in organic synthesis, serving as a useful intermediate in the preparation of various chemical entities. The presence of the iodine substituent enhances its reactivity, making it a valuable starting material for nucleophilic substitution reactions, coupling reactions, and other transformations in pharmaceutical and materials chemistry.
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Ferrocenecarboxylic acid CAS:1271-42-7
Ferrocenecarboxylic acid is an organometallic compound that features a carboxylic acid (-COOH) group attached to the ferrocene framework, which consists of two cyclopentadienyl rings sandwiching a central iron atom. This unique structure imparts distinctive chemical properties and reactivity patterns, making it valuable in materials science, catalysis, and organic synthesis. Ferrocenecarboxylic acid exhibits notable electrochemical behavior due to its redox-active nature, contributing to its application in sensors and energy storage devices. Additionally, its ability to serve as a precursor for various derivatives enhances its significance in developing novel compounds for pharmaceutical and industrial purposes.
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Esculetin CAS:93-35-6
Esculetin, also known as 6,7-dihydroxycoumarin, is a natural compound belonging to the coumarin family. Characterized by its two hydroxyl groups at the 6 and 7 positions, esculetin exhibits a diverse range of biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. It has been studied for its potential therapeutic effects in various ailments such as cardiovascular diseases and cancer. Additionally, esculetin serves as a valuable scaffold for developing novel derivatives with enhanced pharmacological profiles. Its unique chemical structure and bioactivity make it an important compound in medicinal chemistry and natural product research.
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Methyl 2-iodobenzoate CAS:610-97-9
Methyl 2-iodobenzoate is an aromatic ester formed by the esterification of 2-iodobenzoic acid with methanol. This compound features a methyl group attached to the carboxylic acid moiety of the 2-iodobenzoate structure, enhancing its reactivity and solubility in organic solvents. Methyl 2-iodobenzoate is notable for its utility in organic synthesis, where it serves as an important intermediate in various chemical reactions. Due to the presence of the iodine atom, the compound plays a significant role in nucleophilic substitution reactions and cross-coupling reactions, making it valuable in pharmaceuticals, agrochemicals, and materials science.
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Hydrocinnamoyl chloride CAS:645-45-4
Hydrocinnamoyl chloride is an aromatic acyl chloride derived from hydrocinnamic acid, characterized by a carbonyl group (C=O) attached to a hydrocinnamoyl moiety. With the molecular formula C9H9ClO, this compound features a chlorinated alkyl chain, which imparts notable reactivity and utility in organic synthesis. Hydrocinnamoyl chloride serves as a valuable intermediate in the production of various chemicals, including pharmaceuticals and agrochemicals. Its ability to readily undergo acylation reactions makes it a versatile building block for synthesizing more complex molecules and exploring potential applications in materials science and medicinal chemistry.
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3-Phenylpropionic acid CAS:501-52-0
3-Phenylpropionic acid is an organic compound classified as a phenyl-substituted propionic acid. Characterized by a three-carbon chain with a phenyl group attached to the second carbon, this compound possesses both carboxylic acid and aromatic functionalities. Its unique structure offers various chemical properties that make it useful in organic synthesis and medicinal chemistry. 3-Phenylpropionic acid has applications in the production of pharmaceuticals, agrochemicals, and flavoring agents. The compound’s versatility arises from its ability to participate in reactions such as esterification, amidation, and Friedel-Crafts acylation, enabling the formation of complex organic molecules.
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4-Acetylbiphenyl CAS:501-52-0
4-Acetylbiphenyl is an organic compound belonging to the class of biphenyls, characterized by the presence of an acetyl group (-C(=O)CH₃) at the para position of one of the phenyl rings. This compound has garnered attention in synthetic organic chemistry due to its reactivity and potential applications. It serves as an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure provides opportunities for further functionalization, making it a valuable building block in organic synthesis and a subject of interest in material science research.
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2-Chlorophenothiazine CAS:92-39-7
2-Chlorophenothiazine is an organic compound belonging to the phenothiazine family, characterized by a chlorine atom substituted at the second carbon of the phenothiazine structure. This compound features a tricyclic system composed of two benzene rings and a nitrogen-containing thiazine ring, imparting distinctive chemical properties. 2-Chlorophenothiazine exhibits pharmacological significance, particularly in psychiatric medicine, where related compounds are used as antipsychotics. Its unique structure allows for further derivatization, making it a valuable scaffold in medicinal chemistry, drug development, and research into new therapeutic agents targeting various neurological disorders.
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2-Methoxyphenothiazine CAS:1771-18-2
2-Methoxyphenothiazine is an organic compound belonging to the phenothiazine family, characterized by a methoxy group (-OCH₃) positioned at the second carbon of the phenothiazine structure. This compound exhibits notable pharmacological properties, particularly as an antipsychotic and antiemetic agent. The presence of the methoxy substitution enhances its lipophilicity and modifies its interaction with biological targets, making it relevant in medicinal chemistry. 2-Methoxyphenothiazine serves as an important scaffold in drug development, facilitating the synthesis of various derivatives that exhibit therapeutic potential for neurological disorders and other medical conditions.
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3,5-Dimethoxyaniline CAS:10272-07-8
3,5-Dimethoxyaniline is an aromatic amine characterized by the presence of two methoxy groups (-OCH₃) at the 3 and 5 positions of the aniline ring. This compound is notable for its electronic properties, which are significantly influenced by the electron-donating nature of the methoxy substituents. As a result, 3,5-dimethoxyaniline exhibits enhanced reactivity in electrophilic aromatic substitution reactions. The compound finds applications in various fields, including dye synthesis, pharmaceuticals, and organic electronics, serving as a valuable intermediate in the production of functional materials and biologically active compounds.
