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TCI

CAS 101219-73-2

(S)-1-(4-Fluorophenyl)ethan-1-ol TCI F1327

(S)-1-(4-Fluorophenyl)ethan-1-ol TCI F1327

Chemical Identity

Other names
(1S)-1-(4-Fluorophenyl)ethanol · (S)-4-Fluoro-alpha-methylbenzyl Alcohol
CAS No.
101219-73-2
Formula
C8H9FO
Molecular weight
140.16 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(1S)-1-(4-fluorophenyl)ethanol
SMILES
CC(C1=CC=C(C=C1)F)O
InChIKey
PSDSORRYQPTKSV-LURJTMIESA-N
MDL
MDL03092998
PubChem
CID 852997
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(S)-1-(4-Fluorophenyl)ethan-1-ol is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in the development of pharmaceuticals and organic chemicals by enabling the creation of enantiomerically pure compounds. Its chiral nature allows for the synthesis of molecules with specific biological activities, making it an essential tool in modern chemical research. In laboratory settings, it serves as a key reagent in reactions that require precise control over stereochemistry.

The compound's chemical stability and controlled reactivity make it a preferred choice for asymmetric synthesis applications. Its ability to form different isomers is particularly valuable in pharmacological research, where the biological activity of a compound can vary significantly between its enantiomers. The compound's predictable behavior under various reaction conditions enhances its utility in both academic and industrial research environments.

In Indonesian laboratories, (S)-1-(4-Fluorophenyl)ethan-1-ol is commonly used in chemical and pharmaceutical research. It is a key component in studies aimed at developing new compounds with specific biological functions. Many educational and research institutions in Indonesia incorporate this compound into their programs focused on asymmetric synthesis and drug development. Its application supports the advancement of organic chemistry and medicinal chemistry in the region.

  • Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, which are essential in drug development and pharmaceutical research.
  • Organic Chemistry Research: It is widely used in the synthesis of complex organic molecules, supporting the exploration of new chemical structures and reactions.
  • Pharmaceutical Development: Its chiral properties make it suitable for the production of pharmaceuticals with specific biological activities and therapeutic effects.
  • Isomer Studies: The compound's ability to form different isomers is valuable in studying the effects of stereochemistry on molecular function and biological activity.
  • Academic Teaching: It is frequently used in educational settings to demonstrate principles of asymmetric synthesis and chiral compound formation.

Brand TCI
CAS number 101219-73-2
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid accidental exposure. Laboratory personnel should handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is advised to maintain the compound's integrity and effectiveness in research applications.

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