CAS 51419-59-1
:chlorure de (4-méthylphényl)méthanesulfonyle
- P-Tolylmethanesulfonyl Chloride
- 4-Methylbenzylsulfonyl chloride
(4-Methylphenyl)methylsulphonyl chloride
CAS :(4-Methylphenyl)methylsulphonyl chlorideFormule :C8H9ClO2SDegré de pureté :>97%Couleur et forme :SolidMasse moléculaire :204.67386p-Tolylmethanesulfonyl chloride
CAS :Formule :C8H9ClO2SDegré de pureté :95%Couleur et forme :SolidMasse moléculaire :204.6739p-Tolylmethanesulfonyl chloride
CAS :p-Tolylmethanesulfonyl chlorideFormule :C8H9ClO2SDegré de pureté :96%Masse moléculaire :204.67p-Tolyl-methanesulfonyl chloride
CAS :Formule :C8H9ClO2SDegré de pureté :95%Couleur et forme :Chunks,Crystalline PowderMasse moléculaire :204.674-Methylbenzylsulfonyl chloride
CAS :4-Methylbenzylsulfonyl chloride is a nontoxic chemical compound that inhibits the growth of breast cancer cells. It has been shown to react with and destroy RNA, proteins, and enzymes that are involved in cell division. 4-Methylbenzylsulfonyl chloride also has been shown to have antitumour activity in breast cancer cells. This compound is active against the MDA-MB-231 cell line, which is a human breast cancer cell line derived from metastatic mammary adenocarcinoma. The mechanisms of action of 4-methylbenzylsulfonyl chloride include interference with the synthesis of urokinase, an enzyme that plays an important role in tumour proliferation, as well as inhibition of the cyclooxygenase pathway and other biochemical pathways involved in urokinase production. 4-Methylbenzylsulfonyl chloride may also inhibit angiogenesis by inhibiting trypsin or
Formule :C8H9ClO2SDegré de pureté :Min. 95%Masse moléculaire :204.67 g/mol




