(1R)-2-Chloro-1-(3,4-Difluorophenyl)-1-Ethanol

98%

Reagent Code: #231770
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CAS Number 1212376-05-0

science Other reagents with same CAS 1212376-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.59 g/mol
Formula C₈H₇ClF₂O
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its stereochemistry and halogenated aromatic structure make it valuable for constructing active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors (SNRIs), where the (R)-configuration enhances binding affinity and metabolic stability. Also utilized in research settings for asymmetric synthesis and development of novel fluorinated bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,260.00
inventory 250mg
10-20 days ฿5,420.00
inventory 1g
10-20 days ฿13,290.00
(1R)-2-Chloro-1-(3,4-Difluorophenyl)-1-Ethanol
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its stereochemistry and halogenated aromatic structure make it valuable for constructing active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors (SNRIs), where the (R)-configuration enhances binding affinity and metabolic stability. Also ut

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and antidepressants. Its stereochemistry and halogenated aromatic structure make it valuable for constructing active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Commonly employed in the preparation of serotonin and norepinephrine reuptake inhibitors (SNRIs), where the (R)-configuration enhances binding affinity and metabolic stability. Also utilized in research settings for asymmetric synthesis and development of novel fluorinated bioactive molecules.

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