(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate

99%

Reagent Code: #36272
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CAS Number 419563-22-7

science Other reagents with same CAS 419563-22-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.26 g/mol
Formula C₁₁H₁₇NO₈
badge Registry Numbers
MDL Number MFCD18252294
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules. Its unique stereochemistry and functional groups make it valuable for constructing chiral compounds, particularly in the development of antiviral and anticancer drugs. The compound's cyclopentene ring and carboxylate group allow for versatile chemical modifications, enabling the creation of targeted therapeutic agents. Additionally, it is employed in research settings to study enzyme inhibition and receptor binding, contributing to the discovery of new drug candidates. Its role in asymmetric synthesis also highlights its importance in producing enantiomerically pure substances, which are critical for effective and safe medications.

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Test Parameter Specification
Appearance Pale Yellow Powder
Purity 98.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Purity (%) 98.5-100%

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,980.00
inventory 1g
10-20 days ฿17,990.00
inventory 250mg
10-20 days ฿6,600.00
inventory 10g
10-20 days ฿59,990.00

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(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate
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(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules. Its unique stereochemistry and functional groups make it valuable for constructing chiral compounds, particularly in the development of antiviral and anticancer drugs. The compound's cyclopentene ring and carboxylate group allow for versatile chemical modifications, enabling the creation of targeted therapeutic agents. Additionally, it is employed in research settings to study enzyme inhibition and receptor binding, contributing to the discovery of new drug candidates. Its role in asymmetric synthesis also highlights its importance in producing enantiomerically pure substances, which are critical for effective and safe medications.
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