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  • 1 ’1-Bis(diphenylphosphino)ferrocene Palladium(Ⅱ)chloride dichloromethane chloride CAS:95464-05-4

    1 ’1-Bis(diphenylphosphino)ferrocene Palladium(Ⅱ)chloride dichloromethane chloride CAS:95464-05-4

    1,1-Bis(diphenylphosphino)ferrocene Palladium(II) Chloride Dichloromethane Complex, with the chemical formula [Pd(dppf)Cl₂·CH₂Cl₂], is an organometallic compound containing palladium(II) coordinated with the dppf ligand and chlorides in a dichloromethane solvent. It is commonly used in organic synthesis and catalysis.

  • N-(6-bromopyridin-2-yl)thiourea CAS:439578-83-3

    N-(6-bromopyridin-2-yl)thiourea CAS:439578-83-3

    N-(6-Bromopyridin-2-yl)thiourea is a chemical compound characterized by the presence of a thiourea functional group attached to a 6-bromopyridin-2-yl moiety. This compound has garnered interest in medicinal chemistry due to its diverse pharmacological activities and potential therapeutic applications. Its unique structural features offer avenues for designing novel drug candidates with specific biological targets, making it a valuable asset in drug discovery and development.

  • 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL CAS:269409-97-4

    2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL CAS:269409-97-4

    2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, commonly known as TMDBP, is a chemical compound belonging to the class of phenolic boronic esters. Its molecular structure comprises a phenolic hydroxyl group attached to a phenyl ring bearing a boron-containing cyclic ester moiety. This compound holds significance in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a valuable boronic ester reagent. Additionally, its stable cyclic boronate structure and sterically hindered nature make it useful in designing ligands for transition metal-catalyzed reactions and in the development of functional materials.

  • 1-Methyl-4-pyrazole boronic acid pinacol ester CAS:761446-44-0

    1-Methyl-4-pyrazole boronic acid pinacol ester CAS:761446-44-0

    1-Methyl-4-pyrazole boronic acid pinacol ester is a chemical compound categorized as a boronic ester. Its molecular structure consists of a boronic acid moiety attached to a pyrazole ring substituted with a pinacol ester group (-OC(CH₃)₂C(CH₃)₂O-). This compound holds significant importance in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile boronic ester reagent. Additionally, its stability, selective reactivity, and compatibility with various reaction conditions make it valuable in the synthesis of pharmaceutical intermediates, agrochemicals, and functional materials.

  • Cyclopenta[b]pyrrole-3a(1H)-methanol, hexahydro- CAS:1784081-72-6

    Cyclopenta[b]pyrrole-3a(1H)-methanol, hexahydro- CAS:1784081-72-6

    Cyclopenta[b]pyrrole-3a(1H)-methanol, hexahydro- is a fused bicyclic compound with a cyclopenta[b]pyrrole core structure and a hexahydro-1H-pyrrole-3a(1H)-methanol side chain. This molecule is significant in medicinal chemistry due to its potential pharmacological activities. Its unique structure offers opportunities for the development of novel drug candidates, particularly targeting neurological disorders and other diseases where modulation of neurotransmitter receptors and transporters is crucial. Cyclopenta[b]pyrrole-3a(1H)-methanol, hexahydro- serves as a scaffold for medicinal chemists exploring new therapeutic agents with optimized pharmacokinetic properties and reduced side effects.

  • trans-1-(tert-Butoxycarbonyl)-4-(3-(trifluoromethyl)phenyl)pyrrolidine-3-carboxylicacid CAS:169248-97-9

    trans-1-(tert-Butoxycarbonyl)-4-(3-(trifluoromethyl)phenyl)pyrrolidine-3-carboxylicacid CAS:169248-97-9

    Trans-1-(tert-butoxycarbonyl)-4-(3-(trifluoromethyl)phenyl)pyrrolidine-3-carboxylic acid is a complex molecule featuring a pyrrolidine ring substituted with a tert-butoxycarbonyl group at the 1 position and a 3-(trifluoromethyl)phenyl group at the 4 position. This compound holds significance in medicinal chemistry, primarily due to its potential as a pharmacophore in drug design. Its intricate structure presents opportunities for creating novel therapeutic agents with tailored pharmacological properties, particularly targeting pathways implicated in inflammatory diseases, cancer, or central nervous system disorders.

  • (3R,4S)-1-tert-Butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate hydrochloride CAS:1262849-90-0

    (3R,4S)-1-tert-Butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate hydrochloride CAS:1262849-90-0

    (3R,4S)-1-tert-Butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate hydrochloride is a chemical compound characterized by a pyrrolidine ring substituted with an ethyl group at the 3-position and a tert-butyl group at the 1-position. This compound has attracted attention in medicinal chemistry due to its stereochemical configuration and potential pharmacological applications. Its unique arrangement provides avenues for designing novel drug candidates with specific biological targets, making it a valuable asset in drug discovery and development endeavors.

  • Cis-1-tert-butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate hydrochloride CAS:1233501-65-9

    Cis-1-tert-butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate hydrochloride CAS:1233501-65-9

    Cis-1-tert-butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate hydrochloride is a chemical compound distinguished by a pyrrolidine ring substituted with an ethyl group at the 3-position and a tert-butyl group at the 1-position. This compound has garnered attention in medicinal chemistry due to its structural complexity and potential pharmacological applications. Its unique configuration presents opportunities for designing novel drug candidates with specific biological targets, making it a valuable asset in drug discovery and development endeavors.

  • 4-Hydroxyphenylboronic acid pinacol ester CAS:269409-70-3

    4-Hydroxyphenylboronic acid pinacol ester CAS:269409-70-3

    4-Hydroxyphenylboronic acid pinacol ester, also known as 4-HPBA pinacol ester, is a chemical compound falling under the category of boronic esters. Its molecular structure comprises a boronic acid moiety attached to a phenyl ring substituted with a pinacol ester group (-OC(CH₃)₂C(CH₃)₂O-). This compound holds significant importance in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile boronic ester reagent. Additionally, its stability, ease of handling, and compatibility with various reaction conditions make it valuable in the synthesis of pharmaceutical intermediates, natural products, and functional materials.

  • Benzyl N-[2-(piperidin-4-yl)propan-2-yl]carbamate hydrochloride CAS:1057260-89-5

    Benzyl N-[2-(piperidin-4-yl)propan-2-yl]carbamate hydrochloride CAS:1057260-89-5

    Benzyl N-[2-(piperidin-4-yl)propan-2-yl]carbamate hydrochloride is a chemical compound consisting of a carbamate functional group attached to a piperidine ring substituted with a benzyl group at the nitrogen atom and a propyl group at the carbon atom. This compound has sparked interest in medicinal chemistry due to its structural complexity and potential pharmacological applications. Its unique arrangement offers opportunities for designing novel drug candidates with specific biological targets, making it a valuable asset in drug discovery and development endeavors.

  • 9,9-Dimethyl-9H-fluoren-2-yl-boronic acid CAS:333432-28-3

    9,9-Dimethyl-9H-fluoren-2-yl-boronic acid CAS:333432-28-3

    9,9-Dimethyl-9H-fluoren-2-yl-boronic acid, often referred to as DMFBA, is a chemical compound belonging to the class of boronic acids. Its molecular structure features a boronic acid moiety attached to a fluorene scaffold substituted with two methyl groups at the 9-position. This compound holds significant importance in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, where it acts as a versatile boronic acid reagent. Additionally, its rigid and sterically hindered structure makes it valuable in ligand design for transition metal-catalyzed reactions and in the development of functional materials.

  • 4-Carboxyphenylboronic acid CAS:14047-29-1

    4-Carboxyphenylboronic acid CAS:14047-29-1

    4-Carboxyphenylboronic acid, also known as 4-Carboxyphenylboronic acid or 4-CPBA, is a chemical compound belonging to the class of boronic acids. It is characterized by its boronic acid functional group (-B(OH)₂) attached to a phenyl ring substituted with a carboxylic acid (-COOH) group at the para position. This compound finds extensive applications in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Additionally, its ability to bind to diols and sugars has led to its use in the development of sensors for glucose monitoring and in medicinal chemistry for designing enzyme inhibitors and receptor ligands.