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  • PENTAFLUOROPHENYLHYDRAZINE CAS:828-73-9

    PENTAFLUOROPHENYLHYDRAZINE CAS:828-73-9

    Penta-fluorophenylhydrazine is an organic compound characterized by the presence of a hydrazine group attached to a penta-fluorinated phenyl ring. Its chemical formula is C6H4F5N2, and it appears as a colorless to slightly yellow liquid or crystalline solid. This compound is noted for its unique reactivity, particularly in substitution reactions, due to the highly electronegative fluorine atoms that influence its chemical behavior. The presence of multiple fluorine atoms contributes to its stability and potential applications in various fields.

  • 2,4,6-Trichlorophenylhydrazine CAS:5329-12-4

    2,4,6-Trichlorophenylhydrazine CAS:5329-12-4

    2,4,6-Trichlorophenylhydrazine is an organic compound characterized by a phenylhydrazine structure with three chlorine atoms substituted at the 2, 4, and 6 positions on the aromatic ring. It appears as a yellowish to brown solid and is primarily utilized in research and chemical synthesis. This compound is known for its role in various chemical reactions, particularly in the fields of pharmaceuticals and agrochemicals, where it serves as a key intermediate for producing other valuable compounds.

  • PHENYLACETIC ACID HYDRAZIDE CAS:937-39-3

    PHENYLACETIC ACID HYDRAZIDE CAS:937-39-3

    Phenylacetic acid hydrazide is an organic compound with the chemical formula C8H10N2O2. It is a hydrazide derivative of phenylacetic acid, consisting of a phenyl group attached to an acetic acid moiety, which is further linked to a hydrazine group. This compound appears as a white to off-white crystalline solid and is known for its reactivity in various chemical transformations. Phenylacetic acid hydrazide has gained attention in medicinal chemistry due to its potential bioactive properties.

  • TEREPHTHALIC DIHYDRAZIDE CAS:136-64-1

    TEREPHTHALIC DIHYDRAZIDE CAS:136-64-1

    Terephthalic dihydrazide (TPHD) is an organic compound derived from terephthalic acid, featuring two hydrazine functional groups. It appears as a white crystalline solid and is primarily known for its utility in the synthesis of polymers and other chemical derivatives. TPHD acts as a key intermediate in various chemical reactions, particularly in the production of polyamides and other nitrogen-containing compounds. Its unique structure imparts specific properties that make it valuable in materials science and industrial applications.

  • 3-(TRIFLUOROMETHYL)PHENYLHYDRAZINE         CAS:368-78-5

    3-(TRIFLUOROMETHYL)PHENYLHYDRAZINE CAS:368-78-5

    3-(Trifluoromethyl)phenylhydrazine is an organic compound featuring a phenylhydrazine structure with a trifluoromethyl group (-CF₃) positioned at the meta position of the aromatic ring. This compound is known for its unique properties, particularly due to the presence of the trifluoromethyl moiety, which enhances its lipophilicity and reactivity. It is primarily used in chemical synthesis and research, especially in the fields of medicinal chemistry and materials science.

     

  • P-TOLUALDEHYDE 2,4-DINITROPHENYLHYDRAZONE CAS:2571-00-8

    P-TOLUALDEHYDE 2,4-DINITROPHENYLHYDRAZONE CAS:2571-00-8

    p-Tolualdehyde 2,4-dinitrophenylhydrazone is a hydrazone derivative formed from the reaction of p-tolualdehyde and 2,4-dinitrophenylhydrazine. This compound plays a crucial role in organic chemistry as a reagent for the identification and characterization of aldehydes and ketones. The formation of hydrazones helps distinguish these carbonyl compounds due to their unique physical properties, such as distinct melting points and colors. Understanding the synthesis and behavior of p-tolualdehyde 2,4-dinitrophenylhydrazone provides valuable insights into organic reaction mechanisms and enhances techniques for molecular identification.

  • m-Tolyl isocyanate CAS:621-29-4

    m-Tolyl isocyanate CAS:621-29-4

    m-Tolyl isocyanate, an aromatic isocyanate compound, features a m-tolyl group (1-methylphenyl) linked to the isocyanate functional group (-N=C=O). This compound is recognized for its reactivity and serves as a crucial building block in organic synthesis. m-Tolyl isocyanate is commonly used in the production of urea and carbamate derivatives through its reactions with amines and alcohols. Its unique structure allows for various applications in medicinal chemistry, materials science, and agrochemicals, making it an important compound for researchers and industries focused on synthetic methodologies and innovative material development.

  • p-Tolyl isocyanate CAS:622-58-2

    p-Tolyl isocyanate CAS:622-58-2

    p-Tolyl isocyanate, an aromatic isocyanate compound, features a tolyl group (methyl-substituted phenyl) attached to the isocyanate functional group (-N=C=O). This compound is significant in organic synthesis and materials science due to its reactivity and ability to form urea and carbamate derivatives upon reaction with amines and alcohols. p-Tolyl isocyanate serves as a valuable building block for developing pharmaceuticals, agrochemicals, and polymers. Its unique structure enhances its utility in various chemical applications, making it an important compound for researchers and industries focused on innovative material development and synthetic methodologies.

  • O-TOLUALDEHYDE 2,4-DINITROPHENYLHYDRAZONE CAS:1773-44-0

    O-TOLUALDEHYDE 2,4-DINITROPHENYLHYDRAZONE CAS:1773-44-0

    O-Tolualdehyde 2,4-dinitrophenylhydrazone is a derivative produced through the reaction of o-tolualdehyde and 2,4-dinitrophenylhydrazine. This compound is significant in organic chemistry as it enables the identification and characterization of aldehydes. The formation of hydrazones is a crucial method for detecting carbonyl compounds due to their distinct melting points and physical properties. The synthesis serves both analytical and educational purposes, illustrating important concepts like nucleophilic addition and dehydration reactions. Understanding o-tolualdehyde 2,4-dinitrophenylhydrazone contributes to broader applications in organic synthesis and molecular identification techniques.

  • α-Ketoglutaric acid disodium salt	 CAS:305-72-6

    α-Ketoglutaric acid disodium salt CAS:305-72-6

    α-Ketoglutaric acid disodium salt, often referred to as sodium α-ketoglutarate, is a salt derived from α-ketoglutaric acid, an important intermediate in the Krebs cycle. With the molecular formula C₅H₆Na₂O₄, this compound plays a significant role in metabolism and cellular energy production. Sodium α-ketoglutarate is used in various applications, including dietary supplements, food additives, and pharmaceuticals. Its properties promote amino acid metabolism and nitrogen transport, making it valuable in both nutritional and clinical contexts. Understanding its biochemical roles and applications can enhance its utilization in health and wellness.

  • MONOBUTYL PHTHALATE	 CAS:131-70-4

    MONOBUTYL PHTHALATE CAS:131-70-4

    Monobutyl phthalate (MBP), an ester compound derived from phthalic acid, is formed by the esterification of one butanol molecule with phthalic acid. It is primarily used as a plasticizer in polyvinyl chloride (PVC) and other polymer formulations to enhance flexibility, durability, and workability. MBP plays a crucial role in various industrial applications, including adhesives, coatings, and sealants. Although it provides beneficial properties to materials, concerns have arisen regarding its potential health effects, prompting ongoing research into its safety and environmental impact. Understanding MBP’s characteristics and uses is essential for developing safer alternatives in consumer products.

  • Ethyl (pentafluorobenzoyl)acetate CAS:3516-87-8

    Ethyl (pentafluorobenzoyl)acetate CAS:3516-87-8

    Ethyl (pentafluorobenzoyl)acetate is an aromatic compound characterized by the presence of a pentafluorobenzoyl group attached to an ethyl acetate moiety. This compound is notable for its incorporation of multiple fluorine atoms, which significantly influence its chemical properties, including lipophilicity and reactivity. Ethyl (pentafluorobenzoyl)acetate serves as a valuable intermediate in organic synthesis and medicinal chemistry, allowing for the development of various fluorinated compounds. Its distinct structure provides unique advantages in drug design, agrochemicals, and material sciences, making it an important compound for researchers and industrial applications.