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2-Bromoethyl ether (or Bis(2-bromoethyl) ether) is an organobromine compound that is also an ether. It is used in the manufacture of pharmaceuticals and crown ethers . [ 1 ] [ 2 ] [ 3 ]
Bromoethane, also known as ethyl bromide, is a chemical compound of the haloalkanes group. It is abbreviated by chemists as EtBr (which is also used as an abbreviation for ethidium bromide ). This volatile compound has an ether-like odor.
2-Bromoethyl ethyl ether: UN 2341: 3: 1-Bromo-3-methylbutane: UN 2342: 3: Bromomethylpropanes: UN 2343: 3: 2-Bromopentane: UN 2344: 3: Bromopropanes: UN 2345: 3: 3-Bromopropyne: UN 2346: 3: Butanedione: UN 2347: 3: Butyl mercaptans: UN 2348: 3: Butyl acrylates, inhibited UN 2349? (UN No. no longer in use) UN 2350: 3: Butyl methyl ether: UN 2351 ...
Bis(chloroethyl) ether can be used in the synthesis of the cough suppressant fedrilate. It is combined with benzyl cyanide and two molar equivalents of sodamide in a ring-forming reaction. When treated with strong base, it gives divinyl ether, an anesthetic: [5] O(CH 2 CH 2 Cl) 2 + 2 KOH → O(CH=CH 2) 2 + 2 KCl + 2 H 2 O
Bromobenzene is prepared by the action of bromine on benzene in the presence of Lewis acid catalysts such as aluminium chloride or ferric bromide. [3]Bromobenzene is used to introduce a phenyl group into other compounds.
Chemical structure of chloromethyl methyl ether (MOM-Cl) Chloroalkyl ethers are a class of organic compounds with the general structure R-O-(CH 2) n-Cl, characterized as an ether connected to a chloromethyl group via an alkane chain. Chloromethyl methyl ether (CMME) is an ether with the formula C H 3 OCH 2 Cl.
β-Nitrostyrene is a chemical precursor for slimicides and dyes. Specifically bromo-nitrostyrene is obtained upon treatment with bromine followed by partial dehydrohalogenation [2] while 2-nitrobenzaldehyde is obtained by treatment with ozone respectively.
Acrylates are defined by the formula CH 2 =CHCO 2 R, where R can be many groups: Acrylic acid; Methyl acrylate; Ethyl acrylate; 2-Chloroethyl vinyl ether; 2-Ethylhexyl acrylate; Butyl acrylate; Trimethylolpropane triacrylate (TMPTA) The versatility of the resulting polymers is owed to the range of R groups. Structures of some acrylates