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2-(Difluoromethoxy)-5-fluorobenzylamine is a chemical compound characterized by the presence of a benzylamine group and two fluorine atoms attached to a methoxy group. It is recognized for its potential biological activity and is frequently utilized in pharmaceutical research and drug development. The incorporation of fluorine atoms in the molecule enhances its metabolic stability and optimizes its pharmacokinetic properties, making it a valuable component in the synthesis of drug candidates and a significant molecule for medicinal chemistry studies.

1017779-46-2

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1017779-46-2 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
2-(Difluoromethoxy)-5-fluorobenzylamine serves as a key building block in the synthesis of various drug candidates due to its potential to exhibit pharmacological effects. Its unique structure, including the benzylamine group and fluorinated methoxy group, contributes to the compound's biological activity, which is crucial for the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-(Difluoromethoxy)-5-fluorobenzylamine is employed as an important molecule for exploring its potential applications in the treatment of various diseases. The presence of fluorine atoms can improve the compound's metabolic stability, which is a critical factor in the design of effective drugs with enhanced pharmacokinetic properties.
Used in Enhancing Metabolic Stability:
2-(Difluoromethoxy)-5-fluorobenzylamine is used to increase the metabolic stability of drug candidates. The fluorine atoms in the compound can enhance the resistance to metabolic degradation, thereby potentially extending the duration of action and improving the overall efficacy of the drug.
Used in Improving Pharmacokinetic Properties:
2-(Difluoromethoxy)-5-fluorobenzylamine is utilized to optimize the pharmacokinetic properties of drug candidates, including absorption, distribution, metabolism, and excretion. The presence of fluorine atoms can influence these properties, leading to better drug performance and therapeutic outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 1017779-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,7,7 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1017779-46:
(9*1)+(8*0)+(7*1)+(6*7)+(5*7)+(4*7)+(3*9)+(2*4)+(1*6)=162
162 % 10 = 2
So 1017779-46-2 is a valid CAS Registry Number.

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1017779-46-2Downstream Products

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