203922-16-1

Basic information

• Product Name: 1,3-dibromo-2-(2-chloroethoxy)-5-fluorobenzene
• Synonyms: 1,3-dibromo-2-(2-chloroethoxy)-5-fluorobenzene
• CAS NO: 203922-16-1
• Molecular Weight: 332.394
• Mol File: 203922-16-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3-dibromo-2-(2-chloroethoxy)-5-fluorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-dibromo-2-(2-chloroethoxy)-5-fluorobenzene(203922-16-1)
• EPA Substance Registry System: 1,3-dibromo-2-(2-chloroethoxy)-5-fluorobenzene(203922-16-1)

Safety Data

• Hazardous Substances Data: 203922-16-1(Hazardous Substances Data)

Upstream product

• 3570-58-9 2-chloroethyl mesylate 
• 344-20-7 2,6-dibromo-4-fluorophenol 
• 107-04-0 1-Bromo-2-chloroethane 
• 78-93-3 butanone 
• 371-41-5 4-Fluorophenol 

Downstream Products

• 204122-32-7 N-[5-(2-Chloro-ethoxy)-2-fluoro-phenyl]-methanesulfonamide 
• 203922-25-2 4-<2-(biphenyl-3-ylmethylamino)ethoxy>-7-fluoro-3-thiomethyl-1,3-dihydroindol-2-one 
• 203922-24-1 4-(2-cyclohexylmethylaminoethoxy)-7-fluoro-3-thiomethyl-1,3-dihydroindol-2-one 
• 203922-23-0 4-(2-benzylaminoethoxy)-7-fluoro-3-thiomethyl-1,3-dihydroindol-2-one 
• 203921-01-1 4-(2-benzylamino-ethoxy)-7-fluoro-1,3-dihydro-indol-2-one 
• 203922-20-7 1-(2-chloroethoxy)-4-fluoro-3-aminobenzene 
• 245762-36-1 5-fluoro-2,3-dihydrobenzofuran-7-carbaldehyde 
• 203922-19-4 1-(2-Chloroethoxy)-2.6-dibromo-4-fluoro-3-nitrobenzene 

Relevant articles and documents

PHARMACEUTICAL COMPOSITION FOR TREATING DIABETES

Provided is a compound represented by the following general formula (I), or a pharmaceutically acceptable salt thereof. This novel compound has a glycogen-synthase activation ability, but activates a receptor PPAR to a low degree and is highly safe. In th

A practical approach to highly functionalized benzodihydrofurans

A number of aromatic dibromides have been treated with 2-3 equivalents of n-butyllithium in order to initiate two sequential chemical events, a Parham cyclization and an intermolecular reaction with DMF. (C) 2000 Elsevier Science Ltd.

4-AMINOETHOXY INDOLONE DERIVATIVES

A compound of the formula I: STR1 in which Y is hydrogen, halogen or lower alkoxy; R 1 is hydrogen, lower alkyl or aryl(lower) alkyl; R. sub.2 is hydrogen, lower alkyl or--(CH 2) n X p Ar, where X is oxygen or carbonyl; Ar is cycloalkyl, aryl or arylaryl, oxindolyl, benzimidazolyl, indolyl, 2-oxobenzimidazolyl or 2-thioxobenzimidazolyl; or R 1 and R 2, taken together with the nitrogen atom to which they are attached, complete a 3,4-dihydro-1H-isoquinolinyl or 1,3-dihydro-isoindolyl; n is one of the integers 1,2,3, 4,5 or 6; p is one of the integers 0 or 1; or a pharmaceutically acceptable salt thereof are inhibitors of dopamine synthesis and release, useful in the treatment of schizophrenia, Parkinson's Disease, Tourette's Syndrome, alcohol addiction, cocaine addiction, and addiction to analogous drugs.