(R)-2-Chloro-1-(3-chlorophenyl)ethanol

95%

Reagent Code: #74260
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CAS Number 142763-10-8

science Other reagents with same CAS 142763-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.06 g/mol
Formula C₈H₈Cl₂O
badge Registry Numbers
MDL Number MFCD08064294
thermostat Physical Properties
Boiling Point 285°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the synthesis of various pharmaceutical compounds, particularly as an intermediate in the production of chiral drugs. Its stereochemistry makes it valuable for creating enantiomerically pure substances, which are essential for developing medications with specific biological activities. It is often employed in the preparation of beta-blockers and other cardiovascular drugs, where the precise configuration of the molecule is critical for efficacy and safety. Additionally, it finds use in organic synthesis for constructing complex molecules in agrochemicals and fine chemicals, contributing to the development of advanced materials and crop protection agents.

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Test Parameter Specification
Appearance Colorless to light-yellow liquid
Purity 95%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,920.00
inventory 100mg
10-20 days ฿8,640.00

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(R)-2-Chloro-1-(3-chlorophenyl)ethanol
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This chemical is primarily utilized in the synthesis of various pharmaceutical compounds, particularly as an intermediate in the production of chiral drugs. Its stereochemistry makes it valuable for creating enantiomerically pure substances, which are essential for developing medications with specific biological activities. It is often employed in the preparation of beta-blockers and other cardiovascular drugs, where the precise configuration of the molecule is critical for efficacy and safety. Additiona

This chemical is primarily utilized in the synthesis of various pharmaceutical compounds, particularly as an intermediate in the production of chiral drugs. Its stereochemistry makes it valuable for creating enantiomerically pure substances, which are essential for developing medications with specific biological activities. It is often employed in the preparation of beta-blockers and other cardiovascular drugs, where the precise configuration of the molecule is critical for efficacy and safety. Additionally, it finds use in organic synthesis for constructing complex molecules in agrochemicals and fine chemicals, contributing to the development of advanced materials and crop protection agents.

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