39614-62-5

Basic information

• Product Name: Benzenesulfonyl chloride, 3,4,5-trimethoxy-
• CAS NO: 39614-62-5
• Molecular Formula: C9H11ClO5S
• Molecular Weight: 266.702
• Mol File: 39614-62-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenesulfonyl chloride, 3,4,5-trimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonyl chloride, 3,4,5-trimethoxy-(39614-62-5)
• EPA Substance Registry System: Benzenesulfonyl chloride, 3,4,5-trimethoxy-(39614-62-5)

Safety Data

• Hazardous Substances Data: 39614-62-5(Hazardous Substances Data)

Upstream product

• 24313-88-0 3,4,5-Trimethoxyaniline 
• 3086-62-2 3,4,5-trimethoxybenzamide 
• 42543-45-3 3,4,5-trimethoxybenzoyl azide 
• 6307-90-0 3,4,5-trimethoxy-1-nitrobenzene 
• 118-41-2 Eudesmic acid 
• 4521-61-3 3,4,5-Trimethoxybenzoyl chloride 

Downstream Products

• 312299-84-6 4-nitrophenyl-3,4,5-trimethoxybenzenesulfonate 
• 16807-30-0 3,4,5-trimethoxyphenylmercaptan 
• 1569303-96-3 2-(3,4,5-trimethoxyphenylthio)benzoxazole 
• 1313356-70-5 quinolin-4-yl-3,4,5-trimethoxybenzenesulfonate 
• 1313356-78-3 6-fluoro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate 
• 1313356-77-2 6-chloro-2-(3-methoxyphenyl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate 
• 1313356-76-1 2-(2-fluorophenyl)-6-(pyrrolidin-1-yl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate 
• 1313356-75-0 2-(3-methoxyphenyl)-6-(pyrrolidin-1-yl)quinolin-4-yl 3,4,5-trimethoxybenzenesulfonate 
• 1313356-74-9 6-(2-fluorophenyl)-[1,3]dioxolo[4,5-g]quinolin-8-yl 3,4,5-trimethoxybenzenesulfonate 
• 1313356-73-8 6-(3-methoxyphenyl)-[1,3]dioxolo[4,5-g]quinolin-8-yl 3,4,5-trimethoxybenzenesulfonate 
• 1313356-72-7 6-phenyl-[1,3]dioxolo[4,5-g]quinolin-8-yl 3,4,5-trimethoxybenzenesulfonate 
• 1313356-71-6 2-methylquinolin-4-yl 3,4,5-trimethoxybenzenesulfonate 
• 1334246-06-8 (N-(5,8-Dimethyl-9H-carbazol-1-yl)-3,4,5-trimethoxybenzenesulfonamide) 
• 1314324-97-4 N-(4-methoxy-1H-benzo[d]imidazol-7-yl)-3,4,5-trimethoxybenzenesulfonamide 

Relevant articles and documents

Switchable regioselection of C-H thiolation of indoles using different TMS counterions

A switchable regioselectivity in C-H thiolation reaction by simply swapping the counteranions of TMS is reported here for the first time. An exclusive C3-H thiolation of indoles with sodium arylsulfinates was achieved in the presence of TMSCl as a promoter. In contrast, with the use of TMSOTf instead of TMSCl under otherwise identical conditions, a regiospecific C2-H thiolation of indoles was realized with the same set of substrates.

CELL PROLIFERATION INHIBITORS

Compounds having formula (I), inhibit cellular proliferation. Processes for the preparation of the compounds, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds are disclosed.

Arylsulfonanilide phosphates

The invention provides compounds, compositions and methods relating to novel arylsulfonanilide derivatives and their use as pharmacologically active agents. The compositions find particular use as pharmacological agents in the treatment of disease states, particularly cancer, psoriasis, vascular restenosis, infrections, atherosclerosis and hypercholesterolemia, or as lead compounds for the development of such agents.