2,3-Difluorobenzenethiol, also known by its CAS number 130922-39-3, is an organofluorine compound characterized by the presence of a thiol (-SH) group attached to a benzene ring that has two fluorine substituents at the 2 and 3 positions. This compound typically exhibits a colorless to pale yellow liquid form and possesses a distinct odor associated with thiols. The presence of fluorine atoms enhances its reactivity and can influence its physical properties, such as boiling and melting points, compared to non-fluorinated analogs. 2,3-Difluorobenzenethiol is soluble in organic solvents and may have limited solubility in water due to the hydrophobic nature of the benzene ring. It is used in various chemical synthesis processes, particularly in the development of pharmaceuticals and agrochemicals. As with many thiols, it may exhibit moderate toxicity and should be handled with care in a laboratory setting, following appropriate safety protocols.

Benzenethiol, 2,3-difluoro- (9CI)

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2,3-Difluorobenzenethiol is a triazolopyrimidine that is currently in the preclinical phase of development for the treatment of cancer. It has been shown to have an antagonist effect on the pharmacological activity of pyrazolopyrimidines. The systematic optimization and pharmacokinetic properties of 2,3-difluorobenzenethiol have been studied extensively. This drug is orally bioavailable and has good pharmacological properties.

CAS 130922-39-3: Benzenethiol, 2,3-difluoro- (9CI)

2,3-Difluorobenzenethiol

Ref: 3D-FD77841

Benzenethiol, 2,3-difluoro-

Ref: IN-DA000V4C

2,3-Difluorobenzenethiol

Ref: 10-F061702