Methyl 2-(methylamino)-2-phenylacetate

95%

Reagent Code: #202979
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CAS Number 107635-11-0

science Other reagents with same CAS 107635-11-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.21 g/mol
Formula C₁₀H₁₃NO₂
badge Registry Numbers
MDL Number MFCD12148297
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for the introduction of phenyl and methylamino groups into larger compounds, making it valuable in the development of central nervous system agents and local anesthetics. Commonly employed in the synthesis of amphetamine-related compounds and other nitrogen-containing heterocycles. Also utilized in research settings for studying ester hydrolysis and chiral amine formation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,060.00
inventory 1g
10-20 days ฿32,350.00
Methyl 2-(methylamino)-2-phenylacetate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for the introduction of phenyl and methylamino groups into larger compounds, making it valuable in the development of central nervous system agents and local anesthetics. Commonly employed in the synthesis of amphetamine-related compounds and other nitrogen-containing heterocycles. Also utilized in research settings for studying ester hydrolysis and chiral amine f

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for the introduction of phenyl and methylamino groups into larger compounds, making it valuable in the development of central nervous system agents and local anesthetics. Commonly employed in the synthesis of amphetamine-related compounds and other nitrogen-containing heterocycles. Also utilized in research settings for studying ester hydrolysis and chiral amine formation.

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