tert-butyl N-(1-hydroxybutan-2-yl)carbamate

98%

Reagent Code: #215446
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CAS Number 138373-86-1

science Other reagents with same CAS 138373-86-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.25 g/mol
Formula C₉H₁₉NO₃
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. Its structure allows for selective protection of amine functionalities, making it valuable in multi-step synthesis where controlled reactivity is required. Commonly employed in the development of bioactive molecules, including protease inhibitors and other therapeutic agents. The hydroxyl group enables further functionalization, facilitating the construction of complex molecular architectures. Suitable for use in peptide chemistry and medicinal chemistry research due to its stability and ease of deprotection under mild conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,880.00
250mg
10-20 days ฿4,800.00
500mg
10-20 days ฿7,440.00
1g
10-20 days ฿10,400.00
5g
10-20 days ฿38,400.00
tert-butyl N-(1-hydroxybutan-2-yl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. Its structure allows for selective protection of amine functionalities, making it valuable in multi-step synthesis where controlled reactivity is required. Commonly employed in the development of bioactive molecules, including protease inhibitors and other therapeutic agents. The hydroxyl group enables further functionalization, facilitating the construction of complex molecular architectures. Suita

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. Its structure allows for selective protection of amine functionalities, making it valuable in multi-step synthesis where controlled reactivity is required. Commonly employed in the development of bioactive molecules, including protease inhibitors and other therapeutic agents. The hydroxyl group enables further functionalization, facilitating the construction of complex molecular architectures. Suitable for use in peptide chemistry and medicinal chemistry research due to its stability and ease of deprotection under mild conditions.

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