(1,1-dimethyl-3-oxo-propyl)-carbamic acid tert-butyl ester

98%

Reagent Code: #177840
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CAS Number 181646-38-8

science Other reagents with same CAS 181646-38-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD24465551
inventory_2 Storage & Handling
Storage -20 °C, Sealed, Drying, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected amine group allows selective reactions at other functional sites without interference. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine deprotection is required. The tert-butyl ester group offers stability under various reaction conditions and can be removed under mild acidic conditions, making it suitable for multi-step syntheses. Also utilized in the preparation of beta-amino ketone derivatives, which are key motifs in bioactive compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,450.00
inventory 250mg
10-20 days ฿27,650.00
inventory 1g
10-20 days ฿55,970.00

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(1,1-dimethyl-3-oxo-propyl)-carbamic acid tert-butyl ester
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected amine group allows selective reactions at other functional sites without interference. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine deprotection is required. The tert-butyl ester group offers stability under various reaction conditions and can be removed under mild acidic conditions, making it suitable for mu

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected amine group allows selective reactions at other functional sites without interference. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine deprotection is required. The tert-butyl ester group offers stability under various reaction conditions and can be removed under mild acidic conditions, making it suitable for multi-step syntheses. Also utilized in the preparation of beta-amino ketone derivatives, which are key motifs in bioactive compounds.

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