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TCI

CAS 75968-40-0

(R)-1-(4-Chlorophenyl)ethan-1-ol TCI C3881

(R)-1-(4-Chlorophenyl)ethan-1-ol TCI C3881
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Description

(R)-1-(4-Chlorophenyl)ethan-1-ol is a chiral compound widely used in asymmetric synthesis to produce molecules with defined stereochemistry. This chemical serves as a fundamental building block in the creation of biologically active compounds, particularly in pharmaceutical research. Its structure consists of an ethanol backbone connected to a chlorinated phenyl group, making it a versatile reagent for constructing complex organic molecules. In the laboratory, it plays a crucial role in the development of chiral intermediates, enabling precise control over the spatial arrangement of atoms in final products.

The compound's chemical stability under controlled conditions and its reactivity with various reagents make it a preferred choice for synthetic chemists. Its chiral nature allows for the selective synthesis of enantiomers, which is essential in drug development where stereochemistry significantly affects biological activity. The availability of this compound in pure form and in small packaging sizes facilitates its use in both small-scale and mid-sized laboratory experiments, ensuring accessibility for researchers working on diverse projects.

In Indonesian laboratories, (R)-1-(4-Chlorophenyl)ethan-1-ol is commonly utilized in pharmacological studies, drug synthesis, and organic chemistry research. Its importance lies in its ability to provide controlled stereochemical outcomes, which are critical for the development of therapeutics with high specificity and efficacy. Researchers rely on this compound for its reliability and consistency in producing chiral compounds with desired properties.

Laboratory Applications

  • Biological Active Compound Synthesis: This compound is ideal for creating molecules with specific biological activity due to its chiral structure and reactivity.
  • Pharmaceutical Research: It supports the development of new drugs by enabling the synthesis of chiral intermediates with precise stereochemistry.
  • Organic Chemistry Studies: Its use in asymmetric synthesis allows for the exploration of stereochemical effects in complex molecule formation.
  • Enantiomer Selective Synthesis: The compound’s chiral nature makes it suitable for producing enantiomers with specific spatial configurations.
  • Small-Scale Experimental Work: Its availability in small packaging sizes makes it practical for laboratory experiments that require controlled quantities.

Specifications

  • Brand: TCI
  • CAS number: 75968-40-0
  • Category: Chemistry > Asymmetric Synthesis > Chiral Building Blocks
  • Pack sizes: Available in small packaging sizes for laboratory use
  • Physical form: Liquid
  • Storage note: Store in a cool, dry place away from light and incompatible materials

Handling and Storage

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 made of glass or high-density polyethylene to prevent contamination and maintain purity. Due to its chemical reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to incompatible substances like strong oxidizing agents. Ensure proper ventilation in the workspace to minimize inhalation risks. Regular monitoring of storage conditions is advised to maintain the compound’s integrity and ensure safe laboratory practices.

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