enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Di-tert-butyl dicarbonate - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_dicarbonate

    Bottles of di-tert-butyl dicarbonate buildup of internal pressure in sealed containers caused by its slow decomposition to di-tert-butyl carbonate and ultimately tert-butanol and CO 2 in the presence of moisture. For this reason, it is usually sold and stored in plastic bottles rather than glass ones.

  3. Diethyl pyrocarbonate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_pyrocarbonate

    Properties Chemical formula. C 6 H 10 O 5: Molar mass: 162.141 g·mol −1 Appearance Clear, colorless liquid Density: 1.101 g/mL at 25 °C ... Di-tert-butyl dicarbonate

  4. Dicarbonate - Wikipedia

    en.wikipedia.org/wiki/Dicarbonate

    di-tert-butyl dicarbonate (H 3 C−) 3 C−C 2 O 5 −C(−CH 3) 3, also known as Boc anhydride. It is one of the oxocarbon anions, consisting solely of oxygen and carbon. The anion has the formula − O−C(=O)−O−C(=O)−O − or C 2 O 2− 5. Dicarbonate salts are apparently unstable at ambient conditions, but can be made under pressure ...

  5. tert-Butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_alcohol

    tert-Butyl alcohol is used as a solvent, ethanol denaturant, paint remover ingredient, and gasoline octane booster and oxygenate.It is a chemical intermediate used to produce methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) by reaction with methanol and ethanol, respectively, and tert-butyl hydroperoxide (TBHP) by reaction with hydrogen peroxide.

  6. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  7. tert-Butyloxycarbonyl protecting group - Wikipedia

    en.wikipedia.org/wiki/Tert-butyloxycarbonyl...

    tert-Butyloxycarbonyl protecting group. The tert-butyloxycarbonyl protecting group or tert-butoxycarbonyl protecting group [1] (BOC group) is an acid-labile protecting group used in organic synthesis. The BOC group can be added to amines under aqueous conditions using di-tert-butyl dicarbonate in the presence of a base such as sodium hydroxide:

  8. Tricarbonate - Wikipedia

    en.wikipedia.org/wiki/Tricarbonate

    An important example is di-tert-butyl tricarbonate (H 3 C−) 3 C−C 3 O 7 −C(−CH 3) 3, an intermediate in the synthesis of di-tert-butyl dicarbonate. [1] The term tricarbonate is sometimes used for salts that contain three carbonate dianions in their covalent structure or stoichiometric formula, such as cerium tricarbonate Ce 2 (CO 3) 3.

  9. Polycarbonate (functional group) - Wikipedia

    en.wikipedia.org/wiki/Polycarbonate_(functional...

    Di-tert-butyl tricarbonate extrudes carbon dioxide in the presence of various catalysts to form di-tert-butyl dicarbonate. [2] Long-chain carbon dioxide oligomers are likewise expected to decompose exothermically. [3]