N-(2-Phenylethyl)acetamide

98%

Reagent Code: #217454
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CAS Number 877-95-2

science Other reagents with same CAS 877-95-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.22 g/mol
Formula C₁₀H₁₃NO
badge Registry Numbers
MDL Number MFCD00026177
thermostat Physical Properties
Melting Point 53°C
Boiling Point 154°C/0.3kPa
inventory_2 Storage & Handling
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a building block in the development of central nervous system agents due to its structural similarity to phenylethylamine derivatives. Also employed in the synthesis of fragrances and flavoring agents because of its mild, sweet aroma. Its stability and amide functionality make it suitable for use in peptide mimetic research and as a protecting group strategy in multi-step synthesis.

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inventory 5g
10-20 days ฿2,070.00

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N-(2-Phenylethyl)acetamide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a building block in the development of central nervous system agents due to its structural similarity to phenylethylamine derivatives. Also employed in the synthesis of fragrances and flavoring agents because of its mild, sweet aroma. Its stability and amide functionality make it suitable for use in peptide mimetic research and as a protecting group strategy in multi-step

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a building block in the development of central nervous system agents due to its structural similarity to phenylethylamine derivatives. Also employed in the synthesis of fragrances and flavoring agents because of its mild, sweet aroma. Its stability and amide functionality make it suitable for use in peptide mimetic research and as a protecting group strategy in multi-step synthesis.

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