DL-α-Phenylglycine

98%

Reagent Code: #169919
label
Alias DL-α-aminophenacetic acid; DL-2-phenylglycine
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CAS Number 2835-06-5

science Other reagents with same CAS 2835-06-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.16 g/mol
Formula C₈H₉NO₂
badge Registry Numbers
EC Number 220-608-1
MDL Number MFCD00064402
thermostat Physical Properties
Melting Point 290 °C (subl.)(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

DL-α-Phenylglycine is widely used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-lactam antibiotics such as semi-synthetic penicillins and cephalosporins. It serves as a key intermediate in the preparation of side chains that impart specific antimicrobial activity and resistance to β-lactamase enzymes. Due to its ability to form stable derivatives, it is also employed in the resolution of racemic mixtures and in asymmetric synthesis. Additionally, it finds use in the development of enzyme inhibitors and other bioactive molecules where stereochemistry plays a critical role in biological activity.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿260.00
inventory 100g
10-20 days ฿530.00
inventory 500g
10-20 days ฿2,390.00
inventory 2.5kg
10-20 days ฿11,760.00

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DL-α-Phenylglycine
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DL-α-Phenylglycine is widely used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-lactam antibiotics such as semi-synthetic penicillins and cephalosporins. It serves as a key intermediate in the preparation of side chains that impart specific antimicrobial activity and resistance to β-lactamase enzymes. Due to its ability to form stable derivatives, it is also employed in the resolution of racemic mixtures and in asymmetric synthesis. Additionally, it f

DL-α-Phenylglycine is widely used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-lactam antibiotics such as semi-synthetic penicillins and cephalosporins. It serves as a key intermediate in the preparation of side chains that impart specific antimicrobial activity and resistance to β-lactamase enzymes. Due to its ability to form stable derivatives, it is also employed in the resolution of racemic mixtures and in asymmetric synthesis. Additionally, it finds use in the development of enzyme inhibitors and other bioactive molecules where stereochemistry plays a critical role in biological activity.

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