(1R,2S)-Methyl 1-amino-2-vinylcyclopropanecarboxylate 4-methylbenzenesulfonate

98%

Reagent Code: #230435
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CAS Number 862273-27-6

science Other reagents with same CAS 862273-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.3694 g/mol
Formula C₁₄H₁₉NO₅S
badge Registry Numbers
MDL Number MFCD11616272
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its cyclopropane scaffold with defined stereochemistry allows for precise spatial orientation of functional groups, enhancing drug selectivity. The amine and ester functionalities enable further chemical modifications, making it valuable in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Commonly employed in research settings for asymmetric synthesis and optimization of bioactive compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿742.50
inventory 5g
10-20 days ฿2,799.50
(1R,2S)-Methyl 1-amino-2-vinylcyclopropanecarboxylate 4-methylbenzenesulfonate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its cyclopropane scaffold with defined stereochemistry allows for precise spatial orientation of functional groups, enhancing drug selectivity. The amine and ester functionalities enable further chemical modifications, making it valuable in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Commonly employed in research settin

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its cyclopropane scaffold with defined stereochemistry allows for precise spatial orientation of functional groups, enhancing drug selectivity. The amine and ester functionalities enable further chemical modifications, making it valuable in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Commonly employed in research settings for asymmetric synthesis and optimization of bioactive compounds.

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