(S)-()-γ-Hydroxymethyl-γ-butyrolactone

95%

Reagent Code: #234808
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CAS Number 32780-06-6

science Other reagents with same CAS 32780-06-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 116.12 g/mol
Formula C₅H₈O₃
badge Registry Numbers
MDL Number MFCD00066224
thermostat Physical Properties
Boiling Point 110-115°C 0.2mm Hg (Lit.)
inventory_2 Storage & Handling
Storage 2~8°C, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antiviral and antitumor agents. It serves as a key intermediate in the preparation of nucleoside analogs, which are important in drugs targeting HIV, hepatitis B, and certain cancers. Its lactone structure and hydroxymethyl group allow for selective chemical modifications, making it valuable in asymmetric synthesis and the development of biologically active molecules. Also employed in the manufacture of nootropic agents and neuroprotective compounds due to its structural similarity to neurotransmitter precursors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿500.00
inventory 1g
10-20 days ฿1,980.00

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(S)-()-γ-Hydroxymethyl-γ-butyrolactone
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antiviral and antitumor agents. It serves as a key intermediate in the preparation of nucleoside analogs, which are important in drugs targeting HIV, hepatitis B, and certain cancers. Its lactone structure and hydroxymethyl group allow for selective chemical modifications, making it valuable in asymmetric synthesis and the development of biologically active molecules. Also employed in the manufacture of

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antiviral and antitumor agents. It serves as a key intermediate in the preparation of nucleoside analogs, which are important in drugs targeting HIV, hepatitis B, and certain cancers. Its lactone structure and hydroxymethyl group allow for selective chemical modifications, making it valuable in asymmetric synthesis and the development of biologically active molecules. Also employed in the manufacture of nootropic agents and neuroprotective compounds due to its structural similarity to neurotransmitter precursors.

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