(R)-(-)-Phenylsuccinic acid

≥96%,sum of enantiomers

Reagent Code: #37269
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CAS Number 46292-93-7

science Other reagents with same CAS 46292-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.18 g/mol
Formula C₁₀H₁₀O₄
thermostat Physical Properties
Melting Point 173-176℃
Boiling Point 290.62℃ (rough estimate)
inventory_2 Storage & Handling
Density 1.2534 (rough estimate)
Storage room temperature, dry

description Product Description

(R)-(-)-Phenylsuccinic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the production of various optically active compounds, which are essential in the development of enantiomerically pure drugs. Its chiral nature makes it valuable in asymmetric synthesis, where it can be used to induce stereoselectivity in chemical reactions. Additionally, it is employed in the synthesis of complex molecules, including natural products and bioactive compounds, where the specific stereochemistry is crucial for biological activity. In material science, it can be utilized to create chiral polymers or as a precursor for specialty chemicals with specific optical properties. Its applications also extend to analytical chemistry, where it may be used as a standard or reagent in chiral separation techniques.

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inventory 1g
10-20 days ฿14,139.00

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(R)-(-)-Phenylsuccinic acid
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(R)-(-)-Phenylsuccinic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the production of various optically active compounds, which are essential in the development of enantiomerically pure drugs. Its chiral nature makes it valuable in asymmetric synthesis, where it can be used to induce stereoselectivity in chemical reactions. Additionally, it is employed in the synthesis of complex molecules, including natural products and bi

(R)-(-)-Phenylsuccinic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the production of various optically active compounds, which are essential in the development of enantiomerically pure drugs. Its chiral nature makes it valuable in asymmetric synthesis, where it can be used to induce stereoselectivity in chemical reactions. Additionally, it is employed in the synthesis of complex molecules, including natural products and bioactive compounds, where the specific stereochemistry is crucial for biological activity. In material science, it can be utilized to create chiral polymers or as a precursor for specialty chemicals with specific optical properties. Its applications also extend to analytical chemistry, where it may be used as a standard or reagent in chiral separation techniques.

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