(R)-2-(Cyclopent-1-en-1-yl)-2-hydroxy-2-phenylacetic acid

95%

Reagent Code: #228569
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CAS Number 185030-09-5

science Other reagents with same CAS 185030-09-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.25 g/mol
Formula C₁₃H₁₄O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of β-blockers and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure drugs. The hydroxy and carboxylic acid functional groups enable further chemical modifications, such as esterification or amidation, facilitating integration into larger molecular structures. Commonly employed in research settings for exploring new synthetic routes and optimizing drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,820.00
inventory 250mg
10-20 days ฿9,850.00
inventory 1g
10-20 days ฿25,610.00
(R)-2-(Cyclopent-1-en-1-yl)-2-hydroxy-2-phenylacetic acid
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of β-blockers and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure drugs. The hydroxy and carboxylic acid functional groups enable further chemical modifications, such as esterification or amidation, facilitating integration into larger molecular structures. Commonly employed in research settings for

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of β-blockers and other bioactive molecules. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure drugs. The hydroxy and carboxylic acid functional groups enable further chemical modifications, such as esterification or amidation, facilitating integration into larger molecular structures. Commonly employed in research settings for exploring new synthetic routes and optimizing drug candidates.

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