Carbamic acid, butyl-, 2-(acetyloxy)ethyl ester

95%

Reagent Code: #157202
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CAS Number 150699-20-0

science Other reagents with same CAS 150699-20-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.2356 g/mol
Formula C₉H₁₇NO₄
badge Registry Numbers
MDL Number MFCD24581674
thermostat Physical Properties
Boiling Point 304.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.053±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a chemical intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals. It functions as a protecting group carrier for amines due to its ability to form carbamate derivatives. Its acetyl and ester functionalities allow for selective reactions in multi-step synthesis. It is also employed in the development of prodrugs, where controlled release of active amines is required. Additionally, it finds use in the synthesis of polymers and specialty esters where tailored reactivity and stability are needed.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,200.00
inventory 1g
10-20 days ฿42,880.00
inventory 250mg
10-20 days ฿14,400.00

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Carbamic acid, butyl-, 2-(acetyloxy)ethyl ester
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Used primarily as a chemical intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals. It functions as a protecting group carrier for amines due to its ability to form carbamate derivatives. Its acetyl and ester functionalities allow for selective reactions in multi-step synthesis. It is also employed in the development of prodrugs, where controlled release of active amines is required. Additionally, it finds use in the synthesis of polymers and spec

Used primarily as a chemical intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals. It functions as a protecting group carrier for amines due to its ability to form carbamate derivatives. Its acetyl and ester functionalities allow for selective reactions in multi-step synthesis. It is also employed in the development of prodrugs, where controlled release of active amines is required. Additionally, it finds use in the synthesis of polymers and specialty esters where tailored reactivity and stability are needed.

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