N-Benzylglycine ethyl ester

97%

Reagent Code: #216664
label
Alias N-benzylglycine Ethyl
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CAS Number 6436-90-4

science Other reagents with same CAS 6436-90-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.24 g/mol
Formula C₁₁H₁₅NO₂
badge Registry Numbers
EC Number 229-218-6
MDL Number MFCD00009174
thermostat Physical Properties
Boiling Point 140-142 °C10 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.031 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for easy modification in peptide-like frameworks, making it valuable in medicinal chemistry for developing enzyme inhibitors or receptor ligands. Commonly employed in the synthesis of β-lactam antibiotics and other nitrogen-containing heterocycles. Also utilized in asymmetric synthesis due to its chiral compatibility and ability to act as a building block in multistep reactions.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿420.00
inventory 100g
10-20 days ฿1,620.00
inventory 500g
10-20 days ฿8,010.00

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N-Benzylglycine ethyl ester
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for easy modification in peptide-like frameworks, making it valuable in medicinal chemistry for developing enzyme inhibitors or receptor ligands. Commonly employed in the synthesis of β-lactam antibiotics and other nitrogen-containing heterocycles. Also utilized in asymmetric synthesis due to its chiral compatibility and ability to act as a building block in multi

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for easy modification in peptide-like frameworks, making it valuable in medicinal chemistry for developing enzyme inhibitors or receptor ligands. Commonly employed in the synthesis of β-lactam antibiotics and other nitrogen-containing heterocycles. Also utilized in asymmetric synthesis due to its chiral compatibility and ability to act as a building block in multistep reactions.

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