tert-butyl3-chloroazetidine-1-carboxylate

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Reagent Code: #244368
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CAS Number 1537176-17-2

science Other reagents with same CAS 1537176-17-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.66 g/mol
Formula C₈H₁₄ClNO₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure supports the construction of complex molecules where a protected azetidine ring is required. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other sites in the molecule. It is especially valuable in medicinal chemistry for developing protease inhibitors and receptor modulators. The presence of the chlorine atom offers a site for further functionalization through cross-coupling or nucleophilic substitution reactions, enabling the introduction of diverse substituents during drug discovery pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,510.00
inventory 250mg
10-20 days ฿10,840.00
inventory 1g
10-20 days ฿21,670.00
inventory 5g
10-20 days ฿44,840.00
inventory 10g
10-20 days ฿79,300.00
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tert-butyl3-chloroazetidine-1-carboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure supports the construction of complex molecules where a protected azetidine ring is required. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other sites in the molecule. It is especially valuable in medicinal chemistry for developing protease inhibitors and receptor modulators. The presence of the chlorine atom off

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical development. Its structure supports the construction of complex molecules where a protected azetidine ring is required. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other sites in the molecule. It is especially valuable in medicinal chemistry for developing protease inhibitors and receptor modulators. The presence of the chlorine atom offers a site for further functionalization through cross-coupling or nucleophilic substitution reactions, enabling the introduction of diverse substituents during drug discovery pathways.

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