(R)-1-(2-Chlorophenyl)-N-methylethan-1-amine

95%

Reagent Code: #228688
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CAS Number 1213424-79-3

science Other reagents with same CAS 1213424-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.65128 g/mol
Formula C₉H₁₂ClN
badge Registry Numbers
MDL Number MFCD09825522
thermostat Physical Properties
Boiling Point 211.8±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.058±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry, light-proof

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral active ingredients for central nervous system medications. Its stereochemistry makes it valuable in asymmetric synthesis, where the (R)-enantiomer contributes to selective biological activity. Commonly employed in the development of antidepressants and antipsychotic drugs due to its ability to influence receptor binding affinity. Also utilized in research settings for the preparation of structurally complex amines and in the optimization of drug candidates requiring specific enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,090.00
inventory 100mg
10-20 days ฿17,140.00

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(R)-1-(2-Chlorophenyl)-N-methylethan-1-amine
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral active ingredients for central nervous system medications. Its stereochemistry makes it valuable in asymmetric synthesis, where the (R)-enantiomer contributes to selective biological activity. Commonly employed in the development of antidepressants and antipsychotic drugs due to its ability to influence receptor binding affinity. Also utilized in research settings for the preparation of structu

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral active ingredients for central nervous system medications. Its stereochemistry makes it valuable in asymmetric synthesis, where the (R)-enantiomer contributes to selective biological activity. Commonly employed in the development of antidepressants and antipsychotic drugs due to its ability to influence receptor binding affinity. Also utilized in research settings for the preparation of structurally complex amines and in the optimization of drug candidates requiring specific enantiomeric purity.

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