Tert-butyl thietan-3-ylcarbamate

≥95%

Reagent Code: #240205
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CAS Number 943437-98-7

science Other reagents with same CAS 943437-98-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.28 g/mol
Formula C₈H₁₅NO₂S
badge Registry Numbers
MDL Number MFCD18325185
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its protected amine group allows for selective reactions in multi-step synthesis. The tert-butyl carbamate (Boc) protecting group enhances stability during reactions and can be easily removed under mild acidic conditions, making it valuable in peptide and heterocyclic compound synthesis. The thietane ring contributes to structural rigidity and can influence metabolic stability in bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,310.00
inventory 1g
10-20 days ฿32,520.00
inventory 100mg
10-20 days ฿7,750.00
Tert-butyl thietan-3-ylcarbamate
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its protected amine group allows for selective reactions in multi-step synthesis. The tert-butyl carbamate (Boc) protecting group enhances stability during reactions and can be easily removed under mild acidic conditions, making it valuable in peptide and heterocyclic compound synthesis. The thietane ring contributes to structural rigidity and can influence metabolic stability in bioactive

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its protected amine group allows for selective reactions in multi-step synthesis. The tert-butyl carbamate (Boc) protecting group enhances stability during reactions and can be easily removed under mild acidic conditions, making it valuable in peptide and heterocyclic compound synthesis. The thietane ring contributes to structural rigidity and can influence metabolic stability in bioactive molecules.

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