When.com Web Search

  1. Ads

    related to: 2 bromoethyl ethyl ether sds sheet

Search results

  1. Results From The WOW.Com Content Network
  2. 2-Bromoethyl ether - Wikipedia

    en.wikipedia.org/wiki/2-bromoethyl_ether

    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 ]

  3. List of UN numbers 2301 to 2400 - Wikipedia

    en.wikipedia.org/wiki/List_of_UN_numbers_2301_to...

    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 ...

  4. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    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.

  5. 2-Phenylethyl bromide - Wikipedia

    en.wikipedia.org/wiki/2-Phenylethyl_bromide

    2-Phenylethyl bromide is an organobromide with the formula C 6 H 5 CH 2 CH 2 Br. It is a colorless liquid, although older samples appear yellow. Analogous to the preparation of most 1-bromoalkanes, it is prepared by free-radical addition of hydrogen bromide to styrene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo ...

  6. Diethyl ether (data page) - Wikipedia

    en.wikipedia.org/wiki/Diethyl_ether_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. 5 Distillation data. ... log 10 of Diethyl Ether ...

  7. Bis (chloroethyl) ether - Wikipedia

    en.wikipedia.org/wiki/Bis(chloroethyl)_ether

    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

  8. Chloroalkyl ether - Wikipedia

    en.wikipedia.org/wiki/Chloroalkyl_ether

    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.

  9. Bromomethyl ethyl ketone - Wikipedia

    en.wikipedia.org/wiki/Bromomethyl_ethyl_ketone

    Bromomethyl ethyl ketone is a brominated ketone with lachrymatory effects. It was used as a chemical warfare agent in World War I. Bromomethyl ethyl ketone was developed as an alternative to bromoacetone , because acetone , the precursor to bromoacetone, was required for explosives production.