tert-Butyl (2-chloroacetyl)carbamate

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Reagent Code: #152742
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CAS Number 120158-03-4

science Other reagents with same CAS 120158-03-4

blur_circular Chemical Specifications

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Weight 193.63 g/mol
Formula C₇H₁₂ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of beta-lactam antibiotics. It serves as a protecting group for amines during multi-step organic reactions, allowing selective reactivity at other functional sites. Its chloroacetyl group enables further nucleophilic substitution, making it valuable in constructing complex drug molecules. Commonly applied in research settings for developing active pharmaceutical ingredients (APIs) where controlled amine reactivity is required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,050.00
inventory 1g
10-20 days ฿3,000.00
inventory 5g
10-20 days ฿12,930.00
inventory 25g
10-20 days ฿56,190.00

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tert-Butyl (2-chloroacetyl)carbamate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of beta-lactam antibiotics. It serves as a protecting group for amines during multi-step organic reactions, allowing selective reactivity at other functional sites. Its chloroacetyl group enables further nucleophilic substitution, making it valuable in constructing complex drug molecules. Commonly applied in research settings for developing active pharmaceutical ingredients (APIs) where controlled amine reactivit

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of beta-lactam antibiotics. It serves as a protecting group for amines during multi-step organic reactions, allowing selective reactivity at other functional sites. Its chloroacetyl group enables further nucleophilic substitution, making it valuable in constructing complex drug molecules. Commonly applied in research settings for developing active pharmaceutical ingredients (APIs) where controlled amine reactivity is required.

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