(R)-3-Bromo-alpha-methylbenzyl Alcohol

95%

Reagent Code: #70971
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CAS Number 134615-24-0

science Other reagents with same CAS 134615-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.06 g/mol
Formula C₈H₉BrO
badge Registry Numbers
MDL Number MFCD06658929
thermostat Physical Properties
Boiling Point 264.2±15.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals and agrochemicals. Its chiral nature makes it valuable in asymmetric synthesis, where it aids in creating enantiomerically pure substances. It is often employed in the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry for optimal efficacy. Additionally, it finds use in research laboratories for studying stereoselective reactions and developing new catalytic methods. Its role in constructing complex molecular architectures highlights its importance in organic chemistry and drug discovery.

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Test Parameter Specification
Appearance Colorless to light yellow Liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,989.00
inventory 250mg
10-20 days ฿810.00
inventory 5g
10-20 days ฿7,848.00

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(R)-3-Bromo-alpha-methylbenzyl Alcohol
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This chemical is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals and agrochemicals. Its chiral nature makes it valuable in asymmetric synthesis, where it aids in creating enantiomerically pure substances. It is often employed in the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry for optimal efficacy. Additionally, it finds use in research laboratories for studying stereoselective rea

This chemical is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals and agrochemicals. Its chiral nature makes it valuable in asymmetric synthesis, where it aids in creating enantiomerically pure substances. It is often employed in the development of active pharmaceutical ingredients (APIs) that require specific stereochemistry for optimal efficacy. Additionally, it finds use in research laboratories for studying stereoselective reactions and developing new catalytic methods. Its role in constructing complex molecular architectures highlights its importance in organic chemistry and drug discovery.

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