8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

Base Information

Chemical Name:8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline
CAS No.:869984-54-3
Molecular Formula:C₁₈H₁₇BrN₂O₅S₂
Molecular Weight:485.379
Hs Code.:

Synonyms:8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

Suppliers and Price of 8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

There total 3 articles about 8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 14.0%

: 869984-53-2
8-benzenesulfonyloxy-2-methyl-5-N,N-dimethylaminosulfonylquinoline

: 869984-54-3
8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

Guidance literature:: With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 8h; Heating;
DOI:10.1002/chem.200600379

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 869984-54-3
8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / Et₃N / CHCl₃ / 1.5 h / 20 °C

2: 14 percent / N-bromosuccinimide; AIBN / CCl₄ / 8 h / Heating

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); triethylamine; In tetrachloromethane; chloroform;
DOI:10.1002/chem.200600379

Reference yield:

: 349543-92-6
5-(N,N-dimethyl)sulfonamido-8-hydroxy-2-methylquinoline

: 869984-54-3
8-benzenesulfonyloxy-2-bromomethyl-5-N,N-dimethylaminosulfonylquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / Et₃N / CHCl₃ / 1.5 h / 20 °C

2: 14 percent / N-bromosuccinimide; AIBN / CCl₄ / 8 h / Heating

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); triethylamine; In tetrachloromethane; chloroform;
DOI:10.1002/chem.200600379