tert-Butyl methyl(3-oxopropyl)carbamate

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Reagent Code: #151952
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CAS Number 273757-11-2

science Other reagents with same CAS 273757-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₉H₁₇NO₃
badge Registry Numbers
MDL Number MFCD09751791
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry, Lightproof, Inert Gas

description Product Description

tert-Butyl methyl(3-oxopropyl)carbamate is used as a versatile intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It features a tert-butyl carbamate (Boc) protecting group on a tertiary amine with a methyl substituent and a 3-oxopropyl chain, providing an aldehyde functionality that enables selective reactions at the carbonyl site while protecting the amine. The Boc group can be introduced and removed under mild acidic conditions, making it valuable in multi-step syntheses such as peptide, heterocycle, and API development where controlled reactivity, stability, and orthogonal protection are essential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,850.00
inventory 100mg
10-20 days ฿2,980.00
inventory 250mg
10-20 days ฿7,050.00
inventory 500mg
10-20 days ฿14,070.00
inventory 1g
10-20 days ฿18,050.00

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tert-Butyl methyl(3-oxopropyl)carbamate
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tert-Butyl methyl(3-oxopropyl)carbamate is used as a versatile intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It features a tert-butyl carbamate (Boc) protecting group on a tertiary amine with a methyl substituent and a 3-oxopropyl chain, providing an aldehyde functionality that enables selective reactions at the carbonyl site while protecting the amine. The Boc group can be introduced and removed under mild acidic conditions, making it

tert-Butyl methyl(3-oxopropyl)carbamate is used as a versatile intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It features a tert-butyl carbamate (Boc) protecting group on a tertiary amine with a methyl substituent and a 3-oxopropyl chain, providing an aldehyde functionality that enables selective reactions at the carbonyl site while protecting the amine. The Boc group can be introduced and removed under mild acidic conditions, making it valuable in multi-step syntheses such as peptide, heterocycle, and API development where controlled reactivity, stability, and orthogonal protection are essential.

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