(R)-(1-Chloroethyl)benzene

95%

Reagent Code: #229262
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CAS Number 1459-15-0

science Other reagents with same CAS 1459-15-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.61 g/mol
Formula C₈H₉Cl
badge Registry Numbers
MDL Number MFCD20621164
thermostat Physical Properties
Boiling Point 80-81 °C at 17 mmHg
inventory_2 Storage & Handling
Density 1.046±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a chiral intermediate in organic synthesis, especially in the production of enantiomerically pure compounds. Commonly employed in the pharmaceutical industry to prepare drugs where stereochemistry plays a critical role in biological activity. Also utilized in the synthesis of fine chemicals and agrochemicals requiring specific optical configurations. Its chiral center and reactive chloride group enable stereoselective nucleophilic substitution and elimination reactions, making it valuable in constructing complex molecular frameworks.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,750.00
250mg
10-20 days ฿6,720.00
1g
10-20 days ฿18,370.00
5g
10-20 days ฿55,110.00
25g
10-20 days ฿137,770.00
(R)-(1-Chloroethyl)benzene
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Used primarily as a chiral intermediate in organic synthesis, especially in the production of enantiomerically pure compounds. Commonly employed in the pharmaceutical industry to prepare drugs where stereochemistry plays a critical role in biological activity. Also utilized in the synthesis of fine chemicals and agrochemicals requiring specific optical configurations. Its chiral center and reactive chloride group enable stereoselective nucleophilic substitution and elimination reactions, making it valuab

Used primarily as a chiral intermediate in organic synthesis, especially in the production of enantiomerically pure compounds. Commonly employed in the pharmaceutical industry to prepare drugs where stereochemistry plays a critical role in biological activity. Also utilized in the synthesis of fine chemicals and agrochemicals requiring specific optical configurations. Its chiral center and reactive chloride group enable stereoselective nucleophilic substitution and elimination reactions, making it valuable in constructing complex molecular frameworks.

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