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  • 6-Bromoquinoxaline CAS:50998-17-9

    6-Bromoquinoxaline CAS:50998-17-9

    6-Bromoquinoxaline is an organic compound belonging to the quinoxaline family, characterized by a fused bicyclic structure containing two nitrogen atoms. With the molecular formula C8H6BrN2, this compound features a bromine atom at the 6-position of the quinoxaline ring. It typically appears as a yellow to light brown solid. Given its unique structural attributes, 6-bromoquinoxaline has garnered interest in various fields, including medicinal chemistry and materials science, due to its potential biological activity and reactivity.

     

  • 2-FLUORO-3-(TRIFLUOROMETHYL)BENZALDEHYDE CAS:112641-20-0

    2-FLUORO-3-(TRIFLUOROMETHYL)BENZALDEHYDE CAS:112641-20-0

    2-Fluoro-3-(trifluoromethyl)benzaldehyde is an aromatic aldehyde with the molecular formula C9H6F4O. It features a benzene ring substituted with a fluorine atom at the 2-position and a trifluoromethyl group (-CF3) at the 3-position, along with an aldehyde functional group (-CHO). This compound is typically a colorless to pale yellow liquid and is notable for its unique structure that imparts significant reactivity and potential applications in several chemical fields, particularly in organic synthesis and medicinal chemistry.

     

  • Furan-2-carbonyl chloride, tetrahydro- CAS:52449-98-6

    Furan-2-carbonyl chloride, tetrahydro- CAS:52449-98-6

    Furan-2-carbonyl chloride, tetrahydro-, is an organic compound with the molecular formula C6H7ClO2. It features a furan ring that is substituted at the 2-position with a carbonyl chloride moiety and contains a tetrahydro structure. This compound typically appears as a colorless to pale yellow liquid, notable for its reactivity due to the presence of both the carbonyl and chloride functional groups. Its unique structure makes it a valuable intermediate in various chemical synthesis processes.

  • 3-Chloro-4-cyanopyridine CAS:68325-15-5

    3-Chloro-4-cyanopyridine CAS:68325-15-5

    3-Chloro-4-cyanopyridine is a heterocyclic organic compound with the molecular formula C6H4ClN3. It features a pyridine ring substituted with a chlorine atom at the 3-position and a cyano group (-CN) at the 4-position. This compound appears as a white to light yellow solid and is used in various chemical applications due to its unique functional groups, which provide specific reactivity and properties.

     

  • Nicotinamide CAS:98-92-0

    Nicotinamide CAS:98-92-0

    Nicotinamide, also known as niacinamide, is a form of vitamin B3 that plays a crucial role in cellular metabolism and energy production. It is vital for the synthesis of coenzymes NAD and NADP, which are essential for various biochemical reactions in the body. Beyond its metabolic functions, nicotinamide is recognized for its benefits in skincare, including reducing inflammation, improving skin barrier function, and diminishing the appearance of fine lines and hyperpigmentation. Additionally, it has been studied for its potential neuroprotective properties and its role in managing conditions like diabetes and arthritis.

  • N-Methylhomopiperazine CAS:4318-37-0

    N-Methylhomopiperazine CAS:4318-37-0

    N-Methylhomopiperazine is a cyclic organic compound derived from homopiperazine, featuring a methyl group attached to one of its nitrogen atoms. This modification enhances its lipophilicity and alters its pharmacokinetic properties, making it an interesting candidate for medicinal chemistry applications. N-Methylhomopiperazine is known for its potential biological activities, particularly in modulating neurotransmitter systems related to anxiety and depression. The compound’s structural characteristics allow it to serve as a scaffold for the development of various pharmaceuticals, including antidepressants and analgesics. Its ability to interact with different receptor types highlights its significance in drug discovery and therapeutic research.

  • Homopiperazine CAS:505-66-8

    Homopiperazine CAS:505-66-8

    Homopiperazine is a cyclic organic compound that consists of a six-membered ring containing two nitrogen atoms at opposite positions. It can be considered as a derivative of piperazine, where each nitrogen atom in the ring is bonded to a carbon chain, thus extending the structure. This modification enhances its solubility and potentially alters its biological activity. Homopiperazine is of interest in medicinal chemistry due to its application in synthesizing various pharmaceuticals, including antidepressants and anti-anxiety medications. Its ability to interact with neurotransmitter systems makes it a valuable scaffold for drug discovery and development.

  • α-Phenylcyclopentanecarbonyl chloride CAS:17380-62-0

    α-Phenylcyclopentanecarbonyl chloride CAS:17380-62-0

    α-Phenylcyclopentanecarbonyl chloride is an organic compound featuring a cyclopentane ring substituted with both a phenyl group and a carbonyl chloride functional group. This compound serves as an important intermediate in organic synthesis, particularly in the preparation of various carboxylic acids, esters, and amides. The presence of the carbonyl chloride group enhances its reactivity, making it amenable to numerous nucleophilic substitution reactions. Its unique structure also positions it for applications in pharmaceuticals and agrochemicals, where such intermediates are crucial for constructing more complex molecules. Further investigation of this compound may reveal additional reactivity and utility in synthetic chemistry.

  • Glucose pentaacetate CAS:604-68-2

    Glucose pentaacetate CAS:604-68-2

    Glucose pentaacetate is a derivative of glucose, in which all five hydroxyl (-OH) groups of the glucose molecule are acetylated, resulting in an acyclic structure. This compound appears as a colorless, viscous liquid and is primarily used in organic synthesis and research applications. The acetylation of glucose serves to enhance its stability and solubility in organic solvents, making it suitable for various chemical reactions. Additionally, glucose pentaacetate can be employed as a protective group in carbohydrate chemistry, allowing chemists to modify other functional groups without interfering with the sugar moiety’s reactivity.

  • DL-Adrenalin CAS:329-65-7

    DL-Adrenalin CAS:329-65-7

    DL-Adrenalin, also known as epinephrine or adrenaline, is a catecholamine hormone and neurotransmitter produced by the adrenal glands. It plays a critical role in the body’s “fight or flight” response, increasing heart rate, dilating air passages, and enhancing energy production during stressful situations. Clinically, DL-Adrenalin is commonly used in emergency medicine to treat anaphylaxis, cardiac arrest, and severe asthma attacks. Its rapid action helps restore normal cardiovascular function and improve airflow, making it vital in life-threatening situations. Additionally, it has applications in local anesthetics to prolong their effects by constricting blood vessels.

  • β-D-Glucose pentaacetate CAS:604-69-3

    β-D-Glucose pentaacetate CAS:604-69-3

    β-D-Glucose pentaacetate is a derivative of β-D-glucose, wherein all five hydroxyl (-OH) groups are acetylated to form a more hydrophobic and stable compound. This modification enhances the solubility of glucose in organic solvents, making it useful for various synthetic applications. The pentaacetate form is particularly significant in carbohydrate chemistry as it serves as a protective group, allowing selective manipulation of the sugar’s functional groups during chemical reactions. Additionally, β-D-glucose pentaacetate can be employed in studies related to glycoside formation and carbohydrate reactivity, providing insights into the behavior of sugar derivatives in organic synthesis.

  • N-Hydroxy succinimide CAS:6066-82-6

    N-Hydroxy succinimide CAS:6066-82-6

    N-Hydroxy succinimide (NHS) is a chemical compound commonly used in biochemistry and organic chemistry as a coupling agent. Its primary application is in the formation of amide bonds, often facilitating the conjugation of biomolecules such as proteins, peptides, and nucleic acids. NHS reacts with carboxylic acids to produce stable NHS esters, which can subsequently react with amines to form amides. This property makes NHS valuable in various applications, including drug development, immunoassays, and bioconjugation techniques. Furthermore, it enhances the solubility and stability of the resulting products, contributing to the efficiency of biochemical reactions.