(S)-Methyl 5-thioxopyrrolidine-2-carboxylate

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Reagent Code: #60741
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CAS Number 85178-37-6

science Other reagents with same CAS 85178-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.21 g/mol
Formula C₆H₉NO₂S
badge Registry Numbers
MDL Number MFCD20667046
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in the development of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, it is employed in the creation of chiral compounds, aiding in the production of enantiomerically pure drugs. The compound's thioamide group also makes it useful in organic synthesis, where it participates in cyclization and coupling reactions to form complex heterocyclic structures.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿29,340.00
inventory 250mg
10-20 days ฿3,780.00
inventory 1g
10-20 days ฿9,810.00

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(S)-Methyl 5-thioxopyrrolidine-2-carboxylate
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in the development of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, it is employed in the creation of chiral compounds, aiding in the production of enantiomerically pure drugs. The compound's thioamide group also makes it useful in organic synthesis, where it participates in cycli

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure is particularly valuable in the development of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, it is employed in the creation of chiral compounds, aiding in the production of enantiomerically pure drugs. The compound's thioamide group also makes it useful in organic synthesis, where it participates in cyclization and coupling reactions to form complex heterocyclic structures.

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