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  2. DBNPA - Wikipedia

    en.wikipedia.org/wiki/DBNPA

    DBNPA or 2,2-dibromo-3-nitrilopropionamide is a quick-kill biocide that easily hydrolyzes under both acidic and alkaline conditions. It is preferred for its instability in water as it quickly kills and then quickly degrades to form a number of products, depending on the conditions, including ammonia, bromide ions, dibromoacetonitrile, and dibromoacetic acid. [2]

  3. Benzhydryl compounds - Wikipedia

    en.wikipedia.org/wiki/Benzhydryl_compounds

    Ball-and-stick model of diphenylmethane. The benzhydryl compounds are a group of organic compounds whose parent structures include diphenylmethane (which is two benzene rings connected by a single methane), with any number of attached substituents, including bridges.

  4. 2-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopropane

    2-Bromopropane, also known as isopropyl bromide and 2-propyl bromide, is the halogenated hydrocarbon with the formula CH 3 CHBrCH 3. It is a colorless liquid. It is a colorless liquid. It is used for introducing the isopropyl functional group in organic synthesis . 2-Bromopropane is prepared by heating isopropanol with hydrobromic acid .

  5. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Benzyl bromide is an isomer, which has a bromine substituted for one of the hydrogens of toluene's methyl group, and it is sometimes named α-bromotoluene. Preparation [ edit ]

  6. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.

  7. 4-Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-bromobenzaldehyde

    In the first step, two bromine atoms are added to the methyl group of 4-bromotoluene by free radical bromination to form 4-bromobenzal bromide. In the second step, the dibrominated methyl group is hydrolyzed with calcium carbonate , then steam distilled to collect 4-bromobenzaldehyde.

  8. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    Though symptoms of overexposure can begin within 2 days of exposure, typically long-term exposure is more harmful. [ 8 ] In 2008, the U.S. CDC recommended that use of 1-bromopropane as a replacement for perchloroethylene may require adjustment and modification of equipment, improved ventilation, and use of personal protective equipment .

  9. 4-Nitrotoluene - Wikipedia

    en.wikipedia.org/wiki/4-Nitrotoluene

    C 7 H 7 N O 2: Molar mass: 137.138 g·mol −1 Appearance crystalline solid [1] Odor: ... Treatment of 4-nitrotoluene with bromine gives the 4-nitrobenzyl bromide. [9]