Benzyl 3,3-difluoropyrrolidine-1-carboxylate

95%

Reagent Code: #43884
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CAS Number 163457-22-5

science Other reagents with same CAS 163457-22-5

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Weight 241.2339 g/mol
Formula C₁₂H₁₃F₂NO₂
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MDL Number MFCD08437199
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Benzyl 3,3-difluoropyrrolidine-1-carboxylate is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of bioactive compounds. Its structure, featuring a difluorinated pyrrolidine ring, is particularly valuable in the design of drug candidates targeting neurological disorders, such as Parkinson's disease and depression, due to its ability to enhance metabolic stability and bioavailability. Additionally, this compound is employed in the preparation of protease inhibitors, which are critical in the treatment of viral infections like HIV and hepatitis C. Its benzyl ester group also facilitates selective deprotection during multi-step synthetic processes, making it a versatile building block in organic chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,347.00

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Benzyl 3,3-difluoropyrrolidine-1-carboxylate
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Benzyl 3,3-difluoropyrrolidine-1-carboxylate is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of bioactive compounds. Its structure, featuring a difluorinated pyrrolidine ring, is particularly valuable in the design of drug candidates targeting neurological disorders, such as Parkinson's disease and depression, due to its ability to enhance metabolic stability and bioavailability. Additionally, this compound is employed in the preparation of protease

Benzyl 3,3-difluoropyrrolidine-1-carboxylate is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of bioactive compounds. Its structure, featuring a difluorinated pyrrolidine ring, is particularly valuable in the design of drug candidates targeting neurological disorders, such as Parkinson's disease and depression, due to its ability to enhance metabolic stability and bioavailability. Additionally, this compound is employed in the preparation of protease inhibitors, which are critical in the treatment of viral infections like HIV and hepatitis C. Its benzyl ester group also facilitates selective deprotection during multi-step synthetic processes, making it a versatile building block in organic chemistry.

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