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  • 4-BROMOCATECHOL CAS:17345-77-6

    4-BROMOCATECHOL CAS:17345-77-6

    4-Bromocatechol, also known as 4-bromo-1,2-benzenediol, is an organic compound with the molecular formula C6H4BrO2. It features a bromine atom and two hydroxyl groups positioned on a benzene ring. This compound appears as a solid crystalline substance and is of significant interest in organic chemistry due to its reactivity and ability to participate in various chemical transformations. 4-Bromocatechol is primarily used as an intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and in materials science, where its unique properties facilitate the development of diverse functional organic molecules.

  • 4-Butoxyphenol CAS:122-94-1

    4-Butoxyphenol CAS:122-94-1

    4-Butoxyphenol is an organic compound with the molecular formula C10H14O2, characterized by a phenolic structure with a butoxy group (–O–C4H9) attached to the para position of the hydroxyl group (–OH). It typically appears as a colorless to pale yellow liquid or solid. This compound is employed in various industries due to its chemical properties, including as an intermediate in organic synthesis. 4-Butoxyphenol is notable for its applications in pharmaceuticals, agrochemicals, and materials science, where it acts as a stabilizer, surfactant, and a building block for more complex molecules.

  • Cyclopentyl isocyanate CAS:4747-71-1

    Cyclopentyl isocyanate CAS:4747-71-1

    Cyclopentyl isocyanate is an organic compound with the molecular formula C6H11NO. It features a cyclopentane ring with an isocyanate functional group (–N=C=O) that imparts significant reactivity. This colorless to pale yellow liquid is primarily used in the synthesis of various chemical substances, including pharmaceuticals and agrochemicals. Its capacity to participate in nucleophilic addition reactions allows for the functionalization of other organic compounds, making it a valuable intermediate in organic synthesis and polymer chemistry.

  • 1,5-Pentanediol CAS:111-29-5

    1,5-Pentanediol CAS:111-29-5

    1,5-Pentanediol is an organic compound characterized by the formula C5H12O2. It belongs to the family of diols, featuring two hydroxyl (–OH) groups at the first and fifth carbon positions in a five-carbon straight-chain structure. This colorless, hygroscopic liquid is soluble in water and a variety of organic solvents. 1,5-Pentanediol is primarily used in the synthesis of polyesters and polyurethanes, making it valuable in various industrial applications. Additionally, it serves as a solvent, plasticizer, and moisture-retaining agent in cosmetics and personal care products, contributing to its growing importance in the chemical industry.

  • 5-Bromopentan-1-ol CAS:34626-51-2

    5-Bromopentan-1-ol CAS:34626-51-2

    5-Bromopentan-1-ol is an organic compound with the molecular formula C5H11BrO. It features a bromine atom attached to the fifth carbon of a pentanol chain, making it a useful derivative of straight-chain alcohols. This compound appears as a colorless to pale yellow liquid and is primarily employed in organic synthesis. It serves as a reagent in various chemical reactions, particularly in transformations involving halogenation reactions and nucleophilic substitutions. 5-Bromopentan-1-ol is significant for synthesizing a variety of chemical compounds, including pharmaceuticals, agrochemicals, and other functional organic materials.

     

  • 4-tert-Butylcyclohexyl chloroformate CAS:42125-46-2

    4-tert-Butylcyclohexyl chloroformate CAS:42125-46-2

    4-tert-Butylcyclohexyl chloroformate is an organic compound with the molecular formula C12H19ClO2. It features a chloroformate functional group attached to a cyclohexane ring decorated with a tert-butyl group at the 4-position. This colorless to pale yellow liquid is used mainly as a protective group in organic synthesis, particularly in the functionalization of alcohols and amines. Its reactivity allows it to provide a chloroformate moiety, which can be effectively employed in acylation reactions, making it a valuable reagent in medicinal chemistry and the synthesis of complex organic molecules.

     

  • 4-Methoxyphenacyl chloride CAS:2196-99-8

    4-Methoxyphenacyl chloride CAS:2196-99-8

    4-Methoxyphenacyl chloride is an organic compound with the molecular formula C10H9ClO2. It features a phenacyl group substituted with a methoxy group at the para position, resulting in a colorless to pale yellow liquid. This compound is primarily used as a reagent in organic synthesis, particularly in the formation of photoremovable protective groups and in the synthesis of biologically active compounds. Its ability to react with nucleophiles makes it a valuable intermediate in various synthetic pathways, including applications in medicinal chemistry and materials science.

     

  • 2-CHLOROBENZYL CHLOROFORMATE CAS:39545-31-8

    2-CHLOROBENZYL CHLOROFORMATE CAS:39545-31-8

    2-Chlorobenzyl chloroformate is an organic compound with the molecular formula C9H8Cl2O2. Featuring a chloroformate group attached to a 2-chlorobenzyl moiety, this colorless to pale yellow liquid is primarily utilized as a reagent in organic synthesis. It serves as a protective group for alcohols and amines, allowing these functionalities to be selectively masked during complex multi-step reactions. Its reactivity facilitates the formation of carbamates and esters, making it a valuable intermediate in the synthesis of pharmaceuticals and other important chemical compounds.

     

  • Trichloroethanol CAS:115-20-8

    Trichloroethanol CAS:115-20-8

    Trichloroethanol, also known as 2,2,2-trichloroethanol, is a colorless, viscous liquid with a chemical formula of C2HCl3O. It is derived from the chlorination of ethanol and often used as a solvent and intermediate in organic synthesis. Trichloroethanol has a sweet odor and is slightly soluble in water. Primarily, it serves as a precursor to various chemicals and pharmaceuticals. Its ability to act as a sedative and anesthetic also makes it relevant in the medical domain, particularly in the formulation of certain drugs. However, safety precautions are necessary due to its potential toxicity and environmental impact.

  • 4-Methylcyclohexanol CAS:589-91-3

    4-Methylcyclohexanol CAS:589-91-3

    4-Methylcyclohexanol is an organic compound with the molecular formula C7H14O. It features a cyclohexane ring with a methyl group and a hydroxyl group (–OH) at the fourth position. This colorless, oily liquid is often used as a solvent due to its favorable chemical properties. It has a mild odor and low volatility, making it suitable for various applications in the chemical industry. 4-Methylcyclohexanol is primarily utilized in the production of other chemicals and as an intermediate in synthesis, contributing to the manufacture of plasticizers, resins, and surfactants.

     

  • 4-Chloroanisole CAS:623-12-1

    4-Chloroanisole CAS:623-12-1

    4-Chloroanisole, an organic compound with the molecular formula C8H9ClO, features a chloro group substituted at the para position of the anisole molecule. It appears as a colorless liquid with a characteristic sweet, floral odor and is known for its reactivity and versatility in organic synthesis. 4-Chloroanisole is primarily used as a precursor in the synthesis of various chemical compounds, including pharmaceuticals and agrochemicals. Its unique properties make it valuable in several applications across multiple industries, particularly in medicinal chemistry and material science.

     

  • 4-Bromo-2-chlorophenol CAS:3964-56-5

    4-Bromo-2-chlorophenol CAS:3964-56-5

    4-Bromo-2-chlorophenol is an organic compound with the molecular formula C6H4BrClO. This compound features a phenolic hydroxyl group, a bromine atom at the para position, and a chlorine atom at the meta position relative to the hydroxyl group on the benzene ring. It appears as a solid or crystalline substance and is primarily utilized in chemical synthesis as a versatile intermediate. 4-Bromo-2-chlorophenol is significant in pharmaceuticals, agrochemicals, and materials science due to its reactivity and ability to participate in a variety of chemical reactions, including nucleophilic substitutions and coupling reactions.