tert-butyl ((1-(2,6-difluorophenyl)cyclopropyl)methyl)carbamate

90%

Reagent Code: #241803

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.32 g/mol
Formula C₁₅H₁₉F₂NO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

tert-Butyl ((1-(2,6-difluorophenyl)cyclopropyl)methyl)carbamate is a protected amine intermediate featuring a Boc (tert-butyl carbamate) group on a methylamine attached to a 1-(2,6-difluorophenyl)cyclopropane moiety. The cyclopropane ring provides conformational constraint, useful in medicinal chemistry for enhancing potency, selectivity, and metabolic stability in drug candidates. It serves as a building block in the synthesis of bioactive compounds, including potential pharmaceuticals targeting various therapeutic areas such as oncology and central nervous system disorders. The Boc protecting group allows selective manipulation of the amine in multi-step syntheses and can be removed under mild acidic conditions without affecting the core structure.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,356.00
inventory 1g
10-20 days ฿11,484.00
inventory 100mg
10-20 days ฿2,695.00

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tert-butyl ((1-(2,6-difluorophenyl)cyclopropyl)methyl)carbamate
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tert-Butyl ((1-(2,6-difluorophenyl)cyclopropyl)methyl)carbamate is a protected amine intermediate featuring a Boc (tert-butyl carbamate) group on a methylamine attached to a 1-(2,6-difluorophenyl)cyclopropane moiety. The cyclopropane ring provides conformational constraint, useful in medicinal chemistry for enhancing potency, selectivity, and metabolic stability in drug candidates. It serves as a building block in the synthesis of bioactive compounds, including potential pharmaceuticals targeting various

tert-Butyl ((1-(2,6-difluorophenyl)cyclopropyl)methyl)carbamate is a protected amine intermediate featuring a Boc (tert-butyl carbamate) group on a methylamine attached to a 1-(2,6-difluorophenyl)cyclopropane moiety. The cyclopropane ring provides conformational constraint, useful in medicinal chemistry for enhancing potency, selectivity, and metabolic stability in drug candidates. It serves as a building block in the synthesis of bioactive compounds, including potential pharmaceuticals targeting various therapeutic areas such as oncology and central nervous system disorders. The Boc protecting group allows selective manipulation of the amine in multi-step syntheses and can be removed under mild acidic conditions without affecting the core structure.

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