(S)-benzyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate

95%

Reagent Code: #236222
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CAS Number 133464-36-5

science Other reagents with same CAS 133464-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.31 g/mol
Formula C₁₄H₁₉NO₄
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MDL Number MFCD16620549
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-amino alcohol derivatives. Its oxazolidine ring acts as a protective group and stereochemical controller in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemistry is critical. The hydroxymethyl and benzyl functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for constructing complex drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,690.00
inventory 250mg
10-20 days ฿17,390.00
inventory 1g
10-20 days ฿43,460.00
(S)-benzyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-amino alcohol derivatives. Its oxazolidine ring acts as a protective group and stereochemical controller in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemistry is critical. The hydroxymethyl and benzyl functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for constructing co

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-amino alcohol derivatives. Its oxazolidine ring acts as a protective group and stereochemical controller in asymmetric synthesis. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where stereochemistry is critical. The hydroxymethyl and benzyl functionalities allow for further chemical modifications, making it valuable in medicinal chemistry for constructing complex drug candidates.

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