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Catalog Number:
48076
CAS Number:
57842-27-0
1,3-Benzodithiolylium tetrafluoroborate [Hydroxyl protecting agent]
Purity:
≥ 96% (Assay by titration)
Hazmat
Documents
$127.60 /5G
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Product Information

1,3-Benzodithiolylium tetrafluoroborate is a specialized hydroxyl protecting agent, widely utilized in organic synthesis to enhance the stability and reactivity of hydroxyl groups. This compound is particularly valuable in the preparation of complex organic molecules, where selective protection of hydroxyl functionalities is crucial. Its unique properties allow for the efficient blocking of hydroxyl groups, enabling chemists to conduct various reactions without interference from these functional groups.

In addition to its protective capabilities, 1,3-Benzodithiolylium tetrafluoroborate exhibits excellent solubility in polar solvents, making it an ideal choice for reactions in diverse environments. Researchers and industry professionals can leverage this compound in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, where precise control over functional groups is essential. Its effectiveness as a protecting agent not only streamlines synthetic pathways but also enhances overall yields, making it a preferred choice in advanced organic chemistry applications.

CAS Number
57842-27-0
Purity
≥ 96% (Assay by titration)
Molecular Formula
C7H5BF4S2
Molecular Weight
240.04
MDL Number
MFCD00070613
Appearance
Light yellow to brown powder
Conditions
Store at 2 - 8 °C
General Information
CAS Number
57842-27-0
Purity
≥ 96% (Assay by titration)
Molecular Formula
C7H5BF4S2
Molecular Weight
240.04
MDL Number
MFCD00070613
Appearance
Light yellow to brown powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications
1,3-Benzodithiolylium tetrafluoroborate is widely utilized in research focused on
  • Organic Synthesis: This compound serves as a hydroxyl protecting agent, which is crucial in organic synthesis to prevent unwanted reactions during multi-step synthesis processes.
  • Pharmaceutical Development: It is used in the pharmaceutical industry to protect hydroxyl groups in drug molecules, enhancing their stability and bioavailability during formulation.
  • Material Science: In materials chemistry, it aids in the modification of polymer surfaces, improving their chemical resistance and mechanical properties.
  • Analytical Chemistry: This compound is employed in analytical methods to derivatize hydroxyl-containing compounds, facilitating their detection and quantification in complex mixtures.
  • Research in Green Chemistry: Its use aligns with green chemistry principles by enabling selective protection strategies that minimize waste and reduce the need for hazardous reagents.

Citations