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(3,4-Difluoro-5-(4-hydroxypiperidin-1-yl)phenyl)boronic acid is a chemical compound utilized in pharmaceutical research and development. It is known for its potential applications in treating various diseases and conditions, with a particular focus on the development of new medications for neurological and psychiatric disorders. (3,4-Difluoro-5-(4-hydroxypiperidin-1-yl)phenyl)boronic acid features a boronic acid group, which is recognized for its capacity to form stable covalent bonds with specific biomolecules, thereby making it a valuable asset in medicinal chemistry for the design of targeted drug delivery systems. Furthermore, the incorporation of fluorine atoms in the structure of (3,4-Difluoro-5-(4-hydroxypiperidin-1-yl)phenyl)boronic acid is believed to enhance its bioavailability and metabolic stability, positioning it as a promising candidate for drug development.

1704068-71-2

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1704068-71-2 Usage

Uses

Used in Pharmaceutical Research and Development:
(3,4-Difluoro-5-(4-hydroxypiperidin-1-yl)phenyl)boronic acid is used as a research compound for the development of new medications, specifically targeting neurological and psychiatric disorders. Its unique structure, which includes a boronic acid group and fluorine atoms, contributes to its potential as a therapeutic agent, enhancing both its bioavailability and metabolic stability.
Used in Targeted Drug Delivery Systems:
In the field of medicinal chemistry, (3,4-Difluoro-5-(4-hydroxypiperidin-1-yl)phenyl)boronic acid is employed as a component in the design of targeted drug delivery systems. The boronic acid group present in the compound allows for the formation of stable covalent bonds with certain biomolecules, which can be instrumental in the precise delivery of therapeutic agents to their intended sites of action.
Used in Enhancing Bioavailability and Metabolic Stability:
(3,4-Difluoro-5-(4-hydroxypiperidin-1-yl)phenyl)boronic acid is utilized to improve the bioavailability and metabolic stability of medications. The presence of fluorine atoms in its structure is known to enhance these properties, making it an attractive candidate for the development of drugs with better absorption, distribution, metabolism, and excretion profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 1704068-71-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,6 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1704068-71:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*8)+(2*7)+(1*1)=152
152 % 10 = 2
So 1704068-71-2 is a valid CAS Registry Number.

1704068-71-2Upstream product

1704068-71-2Downstream Products

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