(R)-Methyl 2-acetamidopropanoate

95%

Reagent Code: #230059
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CAS Number 19914-36-4

science Other reagents with same CAS 19914-36-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.16 g/mol
Formula C₆H₁₁NO₃
badge Registry Numbers
MDL Number MFCD00080822
thermostat Physical Properties
Boiling Point 251.1°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antibiotics and peptide-based drugs. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Commonly employed in the preparation of β-lactam antibiotics and other bioactive molecules where control of molecular handedness is critical. Also utilized in research for developing protease inhibitors and modified amino acids for drug design.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿148.50
inventory 1g
10-20 days ฿203.50
inventory 5g
10-20 days ฿1,260.00
inventory 10g
10-20 days ฿1,800.00
inventory 25g
10-20 days ฿4,460.00
(R)-Methyl 2-acetamidopropanoate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antibiotics and peptide-based drugs. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Commonly employed in the preparation of β-lactam antibiotics and other bioactive molecules where control of molecular handedness is critical. Also utilized in research for developing protease inhibitors and modified amino acids

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antibiotics and peptide-based drugs. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Commonly employed in the preparation of β-lactam antibiotics and other bioactive molecules where control of molecular handedness is critical. Also utilized in research for developing protease inhibitors and modified amino acids for drug design.

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