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  2. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    These types of chirality are far less common than central chirality. BINOL is a typical example of an axially chiral molecule, while trans-cyclooctene is a commonly cited example of a planar chiral molecule. Finally, helicene possesses helical chirality, which is one type of inherent chirality.

  3. Dichloroiodomethane - Wikipedia

    en.wikipedia.org/wiki/Dichloroiodomethane

    Dichloroiodomethane (DCIM) is a trihalomethane with the chemical formula CHCl 2 I.It is a heavy, nonflammable, transparent pale yellow liquid with a chloroform-like odour. [1]

  4. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Louis Pasteur - pioneering stereochemist. Chirality can be traced back to 1812, when physicist Jean-Baptiste Biot found out about a phenomenon called "optical activity." [10] Louis Pasteur, a famous student of Biot's, made a series of observations that led him to suggest that the optical activity of some substances is caused by their molecular asymmetry, which makes nonsuperimposable mirror ...

  5. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    Chirality (/ k aɪ ˈ r æ l ɪ t i /) is a property of asymmetry important in several branches of science. The word chirality is derived from the Greek χείρ (kheir), "hand", a familiar chiral object. An object or a system is chiral if it is distinguishable from its mirror image; that is, it cannot be superposed (not to be confused with ...

  6. Bromochlorofluoromethane - Wikipedia

    en.wikipedia.org/wiki/Bromochlorofluoromethane

    Bromochlorofluoromethane or fluorochlorobromomethane, is a chemical compound and trihalomethane derivative with the chemical formula C H Br Cl F.As one of the simplest possible stable chiral compounds, it is useful for fundamental research into this area of chemistry. [1]

  7. BINAP - Wikipedia

    en.wikipedia.org/wiki/BINAP

    BINAP (2,2′-bis(diphenylphosphino)-1,1′-binaphthyl) is an organophosphorus compound. This chiral diphosphine ligand is widely used in asymmetric synthesis . It consists of a pair of 2-diphenylphosphino naphthyl groups linked at the 1 and 1′ positions.

  8. Mosher's acid - Wikipedia

    en.wikipedia.org/wiki/Mosher's_acid

    As a chiral derivatizing agent, it reacts with an alcohol or amine [5] of unknown stereochemistry to form an ester or amide. The absolute configuration of the ester or amide is then determined by proton and/or 19 F NMR spectroscopy. Mosher's acid chloride, the acid chloride form, is sometimes used because it has better reactivity.

  9. Chirality timeline - Wikipedia

    en.wikipedia.org/wiki/Chirality_timeline

    Chirality timeline presents a timeline of landmark events that unfold the developments happened in the field of chirality. Many molecules come in two forms that are mirror images of each other, just like our hands. This type of molecule is called chiral. In nature, one of these forms is usually more common than the other.

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