(2,2-Difluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol

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Reagent Code: #36282
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CAS Number 1788873-48-2

science Other reagents with same CAS 1788873-48-2

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Weight 177.19 g/mol
Formula C₈H₁₃F₂NO
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MDL Number MFCD30802952
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(2,2-Difluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its unique structure, featuring difluorinated pyrrolizine, makes it valuable for developing drugs targeting specific enzymes or receptors. This compound is particularly relevant in the design of antiviral and anticancer agents, where its fluorinated moiety enhances metabolic stability and bioavailability. Additionally, it serves as a building block in medicinal chemistry for creating novel therapeutic molecules with improved efficacy and reduced side effects. Its applications extend to research settings, where it is utilized in the study of structure-activity relationships to optimize drug candidates.

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inventory 50mg
10-20 days ฿7,848.00

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(2,2-Difluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol
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(2,2-Difluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its unique structure, featuring difluorinated pyrrolizine, makes it valuable for developing drugs targeting specific enzymes or receptors. This compound is particularly relevant in the design of antiviral and anticancer agents, where its fluorinated moiety enhances metabolic stability and bioavailability. Additionally, i

(2,2-Difluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its unique structure, featuring difluorinated pyrrolizine, makes it valuable for developing drugs targeting specific enzymes or receptors. This compound is particularly relevant in the design of antiviral and anticancer agents, where its fluorinated moiety enhances metabolic stability and bioavailability. Additionally, it serves as a building block in medicinal chemistry for creating novel therapeutic molecules with improved efficacy and reduced side effects. Its applications extend to research settings, where it is utilized in the study of structure-activity relationships to optimize drug candidates.

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