Tert-Butyl N-(4-HYDROXYButyl)Carbamate

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Reagent Code: #241072
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CAS Number 75178-87-9

science Other reagents with same CAS 75178-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.25 g/mol
Formula C₉H₁₉NO₃
badge Registry Numbers
MDL Number MFCD01861334
thermostat Physical Properties
Boiling Point 302.7ºC
inventory_2 Storage & Handling
Density 1.02 g/mL
Storage 2-8ºC

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing protected amino alcohol derivatives. Its hydroxyl and protected amine functionalities allow selective reactions in multi-step syntheses. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine protection is required. Also utilized in polymer chemistry to introduce functional handles for crosslinking or further modification. Stable under a range of reaction conditions, making it suitable for use in peptide mimetics and heterocycle formation.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿162.00
inventory 5g
10-20 days ฿640.00
inventory 25g
10-20 days ฿3,010.00
inventory 1g
10-20 days ฿300.00
inventory 100g
10-20 days ฿9,980.00

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Tert-Butyl N-(4-HYDROXYButyl)Carbamate
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing protected amino alcohol derivatives. Its hydroxyl and protected amine functionalities allow selective reactions in multi-step syntheses. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine protection is required. Also utilized in polymer chemistry to introduce functional handles for crosslinking or further modification. Stable under a range of reac

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing protected amino alcohol derivatives. Its hydroxyl and protected amine functionalities allow selective reactions in multi-step syntheses. Commonly employed in the development of active pharmaceutical ingredients (APIs) where controlled amine protection is required. Also utilized in polymer chemistry to introduce functional handles for crosslinking or further modification. Stable under a range of reaction conditions, making it suitable for use in peptide mimetics and heterocycle formation.

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