(S)-1-(2,3-Difluorophenyl)ethanamine

95%

Reagent Code: #37862
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CAS Number 1415380-62-9

science Other reagents with same CAS 1415380-62-9

blur_circular Chemical Specifications

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Weight 157.1606 g/mol
Formula C₈H₉F₂N
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MDL Number MFCD06761981
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(S)-1-(2,3-Difluorophenyl)ethanamine is primarily used as a chiral building block in the synthesis of pharmaceutical compounds. Its structure, featuring a stereocenter and fluorinated aromatic ring, makes it valuable in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics. The compound’s fluorinated moiety enhances its ability to interact with biological targets, improving metabolic stability and bioavailability. Additionally, it is employed in the production of ligands for asymmetric catalysis, aiding in the creation of enantiomerically pure substances. Its applications extend to research in medicinal chemistry, where it serves as an intermediate in the design of novel therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,784.00

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(S)-1-(2,3-Difluorophenyl)ethanamine
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(S)-1-(2,3-Difluorophenyl)ethanamine is primarily used as a chiral building block in the synthesis of pharmaceutical compounds. Its structure, featuring a stereocenter and fluorinated aromatic ring, makes it valuable in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics. The compound’s fluorinated moiety enhances its ability to interact with biological targets, improving metabolic stability and bioavailability. Additionally, it is employed in the product

(S)-1-(2,3-Difluorophenyl)ethanamine is primarily used as a chiral building block in the synthesis of pharmaceutical compounds. Its structure, featuring a stereocenter and fluorinated aromatic ring, makes it valuable in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics. The compound’s fluorinated moiety enhances its ability to interact with biological targets, improving metabolic stability and bioavailability. Additionally, it is employed in the production of ligands for asymmetric catalysis, aiding in the creation of enantiomerically pure substances. Its applications extend to research in medicinal chemistry, where it serves as an intermediate in the design of novel therapeutic agents.

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