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  2. Bicyclobutane - Wikipedia

    en.wikipedia.org/wiki/Bicyclobutane

    A synthetic approach to bicyclobutane derivatives involves ring closure of a suitably substituted 2-bromo-1-(chloromethyl)cyclopropane with magnesium in THF. [5] Substituted bicyclo[1.1.0]butanes can also be prepared from the reaction of iodo-bicyclo[1.1.1]pentanes with amines, thiols, and sulfinate salts. [6] Bicyclo[1.1.0]butanes are explored ...

  3. Hunsdiecker reaction - Wikipedia

    en.wikipedia.org/wiki/Hunsdiecker_reaction

    Mercuric oxide and bromine convert 3-chlorocyclobutanecarboxylic acid to 1-bromo-3-chlorocyclobutane. This is known as Cristol-Firth modification. This is known as Cristol-Firth modification. [ 14 ] [ 15 ] [ 16 ] The 1,3-dihalocyclobutanes were key precursors to propellanes . [ 17 ]

  4. Over-the-counter drug - Wikipedia

    en.wikipedia.org/wiki/Over-the-counter_drug

    [2] The term over-the-counter (OTC) refers to a medication that can be purchased without a medical prescription. [3] In contrast, prescription drugs require a prescription from a doctor or other health care professional and should only be used by the prescribed individual. [4]

  5. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    2 Li + C 4 H 9 X → C 4 H 9 Li + LiX where X = Cl, Br. The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu. 1-Fluorobutane can be obtained by reacting 1-bromobutane with potassium fluoride in ethylene glycol. [5]

  6. 1-Bromo-3-chloropropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromo-3-chloropropane

    1-Bromo-3-chloropropane is an organohalogen compound with the formula Br(CH 2) 3 Cl. It is a colorless liquid, produced by free-radical addition of hydrogen bromide to allyl chloride. [1] It is used as an alkylating agent to install the –(CH 2) 3 Cl [2] [3] and –(CH 2) 3 – groups. [4] For example, it is a precursor to 4-chlorobutyronitrile.

  7. Bromochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromochlorobenzene

    1-Bromo-2-chlorobenzene: from 2-chloroaniline, via diazotization followed by a Sandmeyer reaction [1] 1-Bromo-3-chlorobenzene: by (3-chlorophenyl)trimethylgermanium by electrophilic substitution [2] [better source needed] 1-Bromo-4-chlorobenzene: From a derivative of (4-bromophenyl)silane using N-bromosuccinimide [3] From 4-chlorophenol using ...

  8. 2C-B-DRAGONFLY - Wikipedia

    en.wikipedia.org/wiki/2C-B-DRAGONFLY

    2C-B-DRAGONFLY (2C-B-DFLY) is a recreational designer drug with psychedelic effects. It can be regarded as the fully aromatic derivative of 2C-B-FLY. 2C-B-DRAGONFLY is stronger than 2C-B or 2C-B-FLY with around 2-3x the potency of 2C-B in animal studies, demonstrating the importance of the fully aromatic benzodifuran ring system for optimum receptor binding at 5-HT 2A, but it is still ...

  9. BCDMH - Wikipedia

    en.wikipedia.org/wiki/BCDMH

    1-Bromo-3-chloro-5,5-dimethylhydantoin (BCDMH or bromochlorodimethylhydantoin) is a chemical structurally related to hydantoin. It is a white crystalline compound with a slight bromine and acetone odor and is insoluble in water, but soluble in acetone .