(S)-Oxazolidine-4-carboxylic acid

95%

Reagent Code: #235738
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CAS Number 45521-08-2

science Other reagents with same CAS 45521-08-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 117.10 g/mol
Formula C₄H₇NO₃
badge Registry Numbers
MDL Number MFCD12911702
thermostat Physical Properties
Boiling Point 295℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.330 g/cm3
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antibiotics such as linezolid and other oxazolidinone-class drugs. Its rigid heterocyclic structure with a stereogenic center enables selective interactions in asymmetric synthesis, making it valuable for creating enantiomerically pure compounds. Also employed in peptidomimetic research to stabilize peptide conformations due to its ability to mimic amino acids while resisting degradation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿44,800.00
inventory 250mg
10-20 days ฿56,000.00
inventory 1g
10-20 days ฿124,800.00
(S)-Oxazolidine-4-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antibiotics such as linezolid and other oxazolidinone-class drugs. Its rigid heterocyclic structure with a stereogenic center enables selective interactions in asymmetric synthesis, making it valuable for creating enantiomerically pure compounds. Also employed in peptidomimetic research to stabilize peptide conformations due to its ability to mimic amino acids while resisting degradation.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antibiotics such as linezolid and other oxazolidinone-class drugs. Its rigid heterocyclic structure with a stereogenic center enables selective interactions in asymmetric synthesis, making it valuable for creating enantiomerically pure compounds. Also employed in peptidomimetic research to stabilize peptide conformations due to its ability to mimic amino acids while resisting degradation.

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