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  • 3-[(Aminoiminomethyl)amino]-4-methylbenzoic acid ethyl ester mononitrate CAS:641569-96-2

    3-[(Aminoiminomethyl)amino]-4-methylbenzoic acid ethyl ester mononitrate CAS:641569-96-2

    3-[(Aminoiminomethyl)amino]-4-methylbenzoic acid ethyl ester mononitrate is a chemical compound that features both amino and nitrate functional groups. This compound is characterized by its unique molecular structure, which includes an aromatic ring with various substituents. Its synthesis involves intricate organic chemistry processes, making it of interest in various fields. The presence of the amino group suggests potential for biological activity, particularly in pharmaceutical applications. The ethyl ester form can influence solubility and bioavailability, enhancing its utility in medicinal chemistry and related areas.

  • 2-Ethyl-5-nitrobenzenamine CAS:20191-74-6

    2-Ethyl-5-nitrobenzenamine CAS:20191-74-6

    2-Ethyl-5-nitrobenzenamine is an organic compound belonging to the class of aromatic amines, characterized by a nitro group and an ethyl substituent on the benzene ring. Its molecular structure consists of a benzene ring with an amino group (NH2) at one position, an ethyl group at another, and a nitro group (NO2) positioned at the meta location relative to the amino group. This specific arrangement imparts unique chemical properties, making 2-ethyl-5-nitrobenzenamine useful in various chemical synthesis applications, including the production of dyes, pharmaceuticals, and agrochemicals.

  • 2-Chloro-4-nitrophenol CAS:619-08-9

    2-Chloro-4-nitrophenol CAS:619-08-9

    2-Chloro-4-nitrophenol is an aromatic compound featuring a chlorine atom and a nitro group attached to a phenolic ring. Specifically, the chlorine is positioned at the ortho position and the nitro group at the para position relative to the hydroxyl group (-OH). This structural arrangement imparts unique chemical properties, making 2-chloro-4-nitrophenol valuable in various applications. It is primarily utilized in organic synthesis as an intermediate for producing dyes, agrochemicals, and pharmaceuticals due to its reactivity and ability to undergo further chemical transformations.

  • 2-Amino-5-iodobenzoic acid CAS:5326-47-6

    2-Amino-5-iodobenzoic acid CAS:5326-47-6

    2-Amino-5-iodobenzoic acid is an aromatic compound characterized by the presence of an amino group (NH2) and a carboxylic acid group (COOH) on a benzene ring, along with an iodine substituent. The amino group is located at the ortho position relative to the carboxylic acid, while the iodine atom is positioned at the para location. This unique structural configuration imparts distinctive chemical properties to the compound. 2-Amino-5-iodobenzoic acid is primarily used as an intermediate in organic synthesis and has applications in pharmaceuticals, agrochemicals, and materials science.

  • 2-Amino-4-fluorobenzoic acid CAS:446-32-2

    2-Amino-4-fluorobenzoic acid CAS:446-32-2

    2-Amino-4-fluorobenzoic acid is an aromatic organic compound characterized by the presence of an amino group (-NH2) and a carboxylic acid group (-COOH) on a benzene ring, with a fluorine atom located at the para position relative to the amino group. This unique structural arrangement imparts distinct chemical properties to the compound, making it useful in various applications. 2-Amino-4-fluorobenzoic acid serves as an important intermediate in organic synthesis, playing a crucial role in the production of pharmaceuticals, agrochemicals, and other specialized chemicals due to its reactivity.

  • 2,3-Dichlorophenoxyacetic acid CAS:2976-74-1

    2,3-Dichlorophenoxyacetic acid CAS:2976-74-1

    2,3-Dichlorophenoxyacetic acid (2,3-DCPA) is an aromatic compound that features two chlorine atoms and a phenoxy group attached to a carboxylic acid. It is primarily known as a herbicide and plant growth regulator in agricultural applications. The compound’s structural characteristics enhance its ability to mimic natural plant hormones, leading to selective herbicidal activity against broadleaf weeds while having minimal effects on grasses. 2,3-DCPA’s effectiveness and relatively low toxicity profile make it a valuable tool in modern agriculture.

  • 4-Bromo-2-Methyl benzoic acid CAS:68837-59-2

    4-Bromo-2-Methyl benzoic acid CAS:68837-59-2

    4-Bromo-2-methylbenzoic acid is an aromatic carboxylic acid featuring a bromine atom and a methyl group attached to a benzene ring. The compound’s molecular structure consists of a para-bromine substitution and an ortho-methyl group with respect to the carboxylic acid functional group. This specific arrangement contributes to its unique chemical properties, making it a valuable intermediate in organic synthesis. Due to its reactivity and ability to undergo various chemical transformations, 4-bromo-2-methylbenzoic acid finds applications in pharmaceuticals, agrochemicals, and materials science.

  • 4-Chloro-3-nitrobenzoic acid CAS:96-99-1

    4-Chloro-3-nitrobenzoic acid CAS:96-99-1

    4-Chloro-3-nitrobenzoic acid is a chlorinated aromatic compound that features both a nitro group and a carboxylic acid functional group on a benzene ring. The chlorine atom is positioned at the para position relative to the carboxylic acid, while the nitro group occupies the meta position. This specific arrangement contributes to its distinct chemical properties and reactivity. 4-Chloro-3-nitrobenzoic acid is used in various synthetic applications, particularly in the fields of pharmaceuticals and agrochemicals, where it serves as an important intermediate for producing complex organic molecules.

  • 3-Bromo-5-nitrobenzotrifluoride CAS:630125-49-4

    3-Bromo-5-nitrobenzotrifluoride CAS:630125-49-4

    3-Bromo-5-nitrobenzotrifluoride is a halogenated aromatic compound featuring a bromine atom and a nitro group on the benzene ring, along with three trifluoromethyl groups. Its unique chemical structure makes it a valuable reagent in organic synthesis and materials science. The presence of both electron-withdrawing and electron-donating groups influences its reactivity, making it suitable for various chemical transformations.

  • 2-Chloro-4-methylsulphonylbenzoic acid            CAS:53250-83-2

    2-Chloro-4-methylsulphonylbenzoic acid CAS:53250-83-2

    2-Chloro-4-methylsulfonylbenzoic acid is an organic compound characterized by a benzoic acid structure with a chlorine atom and a methylsulfonyl group attached to the ortho and para positions, respectively. This compound typically appears as a white crystalline solid and is valued for its unique chemical properties, which arise from the presence of both the chloro and sulfonyl groups. It serves as an important intermediate in chemical synthesis and has diverse applications across pharmaceuticals, agrochemicals, and materials science.

     

  • Methyl 2-chloroacetoacetate CAS:4755-81-1

    Methyl 2-chloroacetoacetate CAS:4755-81-1

    Methyl 2-chloroacetoacetate is an organic compound with the molecular formula C5H7ClO3. It appears as a colorless to pale yellow liquid and features a chloro substituent, which enhances its reactivity in various chemical reactions. This compound is mainly used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for diverse transformations, making it a valuable building block in synthetic chemistry.

  • 3-Cyclohexenecarboxylic acid CAS:4771-80-6

    3-Cyclohexenecarboxylic acid CAS:4771-80-6

    3-Cyclohexenecarboxylic acid is an organic compound characterized by a cyclohexene ring with a carboxylic acid functional group attached at the third position. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. This compound is known for its unique reactivity due to the presence of both the cyclohexene ring and the carboxylic acid group, making it useful in various chemical synthesis processes. Its applications span multiple industries, including pharmaceuticals, agrochemicals, and materials science, where it serves as an intermediate or building block in various reactions.