4-Methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester

CAS: 141699-59-4

Ref. 3D-FM43636

Product Information

• Name: 4-Methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester
• Synonyms: 1,1-Dimethylethyl 4-[(methylsulfonyl)oxy]-1-piperidinecarboxylate, 1-(tert-Butoxycarbonyl)-4-methanesulfonyloxypiperidine, 1-(tert-Butoxycarbonyl)-4-piperidinyl methanesulfonate, 1-Boc-4-(methylsulfonyloxy)piperidine, 1-Boc-4-Methanesulfonyloxy-Piperidine, 1-Piperidinecarboxylic acid, 4-[(methylsulfonyl)oxy]-, 1,1-dimethylethyl ester, 1-tert-Butoxycarbonyl-4-methylsulfonyloxypiperidine, 4-Methanesulfonyloxy-Piperidine-1-Carboxylic Acid Tert-Butyl Ester, 4-Methanesulfonyloxypiperidine-1-carboxylic acid tert-butyl ester, 4-[(Methylsulfonyl)oxy]piperidine-1-carboxylic acid tert-butyl ester, N-(Tert-Butoxycarbonyl)Piperidin-4-Yl Mesylate, N-BOC-4-(methanesulfonyloxy)piperidine, N-Boc-4-mesyloxypiperidine, Tert-Butyl 4-[(Methylsulfonyl)Oxy]Piperidine-1-Carboxylate, tert-Butyl 4-(methanesulfonyloxy)piperidine-1-carboxylate, tert-Butyl 4-(methylsulfonyloxy)piperidin-1-carboxylate, tert-Butyl 4-methylsulfonyloxy-1-piperidinecarboxylate
• CAS: 141699-59-4

Description

4-Methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester is a multi-kinase inhibitor that inhibits the activity of enzymes involved in cellular proliferation and tumor growth. It is a nucleophilic compound that reacts with serotonergic receptors, including 5HT2A. The pharmacokinetic properties of 4-methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester have been studied and found to be similar to those of regorafenib. This drug has been shown to be effective against various cancer cells and is being investigated as a possible treatment for different types of cancer.

• Brand: Biosynth

Chemical properties

• Molecular weight: 279.35 g/mol
• Formula: C₁₁H₂₁NO₅S
• Purity: Min. 95%
• InChI: InChI=1S/C11H21NO5S/c1-11(2,3)16-10(13)12-7-5-9(6-8-12)17-18(4,14)15/h9H,5-8H2,1-4H3
• InChI key: InChIKey=WOEQSXAIPTXOPY-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)N1CCC(OS(C)(=O)=O)CC1