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2,3-Difluoro-4-ethoxybenzeneboronic acid CAS:212386-71-5

2,3-Difluoro-4-ethoxybenzeneboronic acid is a notable compound in the realm of organic chemistry, characterized by its distinct chemical structure and potential applications in synthetic methodologies and material science. Possessing the dual functionality of both boronic acid and fluoroalkoxybenzene moieties, this molecule exhibits unique reactivity and versatility, making it an intriguing building block for the synthesis of complex organic compounds and functional materials. Understanding the structural attributes and chemical behavior of 2,3-Difluoro-4-ethoxybenzeneboronic acid is pivotal for advancing research in organic synthesis, materials chemistry, and related scientific domains. 2,3-Difluoro-4-ethoxybenzeneboronic acid serv


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Application and Effect:

(S)-(+)-α,α-Diphenyl-2-pyrrolidinemethanol serves as a prominent chiral auxiliary in asymmetric synthesis, enabling the construction of intricate molecules with specific stereochemistry. The presence of the pyrrolidine ring and phenyl moieties imparts distinctive steric and electronic effects to the compound, facilitating precise control over stereochemical outcomes in chemical reactions. By exploring its utility in various asymmetric transformations like asymmetric oxidations, asymmetric acylations, and asymmetric additions, researchers can exploit its versatility as a valuable reagent for producing enantiomerically pure molecules and pharmaceutical compounds. Research on the synthesis and applications of (S)-(+)-α,α-Diphenyl-2-pyrrolidinemethanol aims to elucidate its significance as a pivotal chiral building block in organic chemistry and its utility as a versatile reagent in the creation of bioactive molecules. By investigating its reactivity in diverse reaction types, characterizing its stereochemical features, and evaluating its performance in asymmetric catalysis, scientists can unveil innovative approaches for utilizing this compound in the development of chiral drugs, agrochemicals, and advanced materials for various purposes. The distinctive stereochemistry and synthetic adaptability of (S)-(+)-α,α-Diphenyl-2-pyrrolidinemethanol offer promising opportunities for researchers to advance studies in asymmetric synthesis, medicinal chemistry, and chemical biology. Through comprehensive investigations into its synthesis, stereochemical control, and applications in enantioselective catalysis, scientists can contribute to the discovery of novel synthetic techniques and the design of chiral compounds with enhanced biological activities. By exploring the properties and potential applications of (S)-(+)-α,α-Diphenyl-2-pyrrolidinemethanol, researchers can drive innovation in organic synthesis, drug development, and related disciplines, leading to the creation of novel chiral reagents and pharmaceutical candidates with therapeutic value.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C8H9BF2O3
Assay 99%
Appearance white powder
CAS No.  212386-71-5
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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