164062-84-4

Basic information

• Product Name: (1R,2S)-fluorocyclopropanaMine para toluenesulfonate
• Synonyms: (1R,2S)-fluorocyclopropanaMine para toluenesulfonate
• CAS NO: 164062-84-4
• Molecular Formula: C10H14FNO3S
• Molecular Weight: 247.2864632
• EINECS: -0
• Mol File: 164062-84-4.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1R,2S)-fluorocyclopropanaMine para toluenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-fluorocyclopropanaMine para toluenesulfonate(164062-84-4)
• EPA Substance Registry System: (1R,2S)-fluorocyclopropanaMine para toluenesulfonate(164062-84-4)

Safety Data

• Hazardous Substances Data: 164062-84-4(Hazardous Substances Data)

Usage

Description

(1R,2S)-Fluorocyclopropanamine para toluenesulfonate is a chemical compound that features a cyclopropane ring with a fluorine substituent and an attached para toluenesulfonate group. (1R,2S)-Fluorocyclopropanamine para toluenesulfonate is known for its unique structural features and reactivity, which make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals.

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
(1R,2S)-Fluorocyclopropanamine para toluenesulfonate is utilized as an intermediate in the production of various pharmaceuticals and agrochemicals. Its cyclopropane ring and fluorine substituent contribute to the development of new molecules with potential therapeutic or pesticidal properties.
Used in Medicinal Chemistry and Drug Discovery:
In the field of medicinal chemistry, (1R,2S)-Fluorocyclopropanamine para toluenesulfonate is employed as a building block for the design and synthesis of novel drug candidates. Its unique structure allows for the exploration of new chemical space and the development of compounds with improved pharmacological profiles.
Used in Material Science and Catalysis:
(1R,2S)-Fluorocyclopropanamine para toluenesulfonate may also find applications in material science and catalysis due to its reactive nature and the potential for its cyclopropane ring to participate in various chemical transformations. This could lead to the development of new materials with specific properties or the creation of more efficient catalytic processes.