(R)-2-Hydroxy-2-(2-methoxyphenyl)acetic acid

98%

Reagent Code: #228950
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CAS Number 4023-92-1

science Other reagents with same CAS 4023-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.17 g/mol
Formula C₉H₁₀O₄
badge Registry Numbers
MDL Number MFCD20645155
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of anticoagulant drugs. Its enantiomerically pure structure makes it valuable for asymmetric synthesis, where it helps control stereochemistry in complex molecules. Commonly employed in the development of vitamin K antagonists, such as certain coumarin derivatives, due to its ability to mimic key structural elements in biologically active compounds. Also utilized in research settings for the preparation of enzyme inhibitors and receptor ligands where stereochemistry plays a critical role in activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,490.00
inventory 1g
10-20 days ฿14,800.00
inventory 5g
10-20 days ฿51,780.00
(R)-2-Hydroxy-2-(2-methoxyphenyl)acetic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of anticoagulant drugs. Its enantiomerically pure structure makes it valuable for asymmetric synthesis, where it helps control stereochemistry in complex molecules. Commonly employed in the development of vitamin K antagonists, such as certain coumarin derivatives, due to its ability to mimic key structural elements in biologically active compounds. Also utilized in research settings for the preparation of e
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the preparation of anticoagulant drugs. Its enantiomerically pure structure makes it valuable for asymmetric synthesis, where it helps control stereochemistry in complex molecules. Commonly employed in the development of vitamin K antagonists, such as certain coumarin derivatives, due to its ability to mimic key structural elements in biologically active compounds. Also utilized in research settings for the preparation of enzyme inhibitors and receptor ligands where stereochemistry plays a critical role in activity.
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