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  2. Dimethylformamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylformamide

    The catalytic mechanism entails reversible formation of an imidoyl chloride (also known as the 'Vilsmeier reagent'): [27] [28] DMF penetrates most plastics and makes them swell. Because of this property DMF is suitable for solid phase peptide synthesis and as a component of paint strippers. DMF is used as a solvent to recover olefins such as 1 ...

  3. Digital microfluidics - Wikipedia

    en.wikipedia.org/wiki/Digital_microfluidics

    Organic reagents are not commonly used in DMF because they tend to wet the DMF device and cause flooding; however synthesis of organic reagents can be achieved through DMF techniques by carrying the organic reagents through an ionic liquid droplet, thus preventing the organic reagent from flooding the DMF device. [77]

  4. Droplet-based microfluidics - Wikipedia

    en.wikipedia.org/wiki/Droplet-based_Microfluidics

    Droplet formation using a flow focusing device. [17] Diagram of flow focusing droplet formation device commonly used in microfluidic devices. Liquid flowing in from the left is pinched off into droplets by an oil flowing in from the top and bottom. [10] Two stream reagent addition using a flow focusing approach with a planar chip format. [18]

  5. Bouveault aldehyde synthesis - Wikipedia

    en.wikipedia.org/wiki/Bouveault_aldehyde_synthesis

    The first step of the Bouveault aldehyde synthesis is the formation of the Grignard reagent. Upon addition of a N , N -disubstituted formamide (such as dimethylformamide ) a hemiaminal is formed, which can easily be hydrolyzed into the desired aldehyde.

  6. Vilsmeier reagent - Wikipedia

    en.wikipedia.org/wiki/Vilsmeier_reagent

    The Vilsmeier reagent is an organic compound with the formula [(CH 3) 2 NCHCl]Cl. It is a salt consisting of the N,N-dimethyl­iminium cation ([(CH 3) 2 N=CHCl] +) and chloride anion. Depending on the particular reaction, the anion can vary. In typical POCl 3-based reactions, the anion is PO 2 Cl 2 −.

  7. Vilsmeier–Haack reaction - Wikipedia

    en.wikipedia.org/wiki/Vilsmeier–Haack_reaction

    The reaction of a substituted amide with phosphorus oxychloride gives a substituted chloroiminium ion (2), also called the Vilsmeier reagent. The initial product is an iminium ion (4b), which is hydrolyzed to the corresponding ketone or aldehyde during workup. [7] The Vilsmeier–Haack reaction

  8. Mehler reaction - Wikipedia

    en.wikipedia.org/wiki/Mehler_reaction

    In scientific literature, the Mehler reaction often is used interchangeably with the Water-Water Cycle [2] to refer to the formation of H 2 O 2 by photosynthesis. Sensu stricto, the Water Water Cycle encompasses the Hill reaction, in which water is split to form oxygen, as well as the Mehler Reaction, in which oxygen is reduced to form H 2 O

  9. Water cycle - Wikipedia

    en.wikipedia.org/wiki/Water_cycle

    The ocean plays a key role in the water cycle as it is the source of 86% of global evaporation. [2] The water cycle involves the exchange of energy, which leads to temperature changes. When water evaporates, it takes up energy from its surroundings and cools the environment. When it condenses, it releases energy and warms the environment.