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  2. Dibenzyl ether - Wikipedia

    en.wikipedia.org/wiki/Dibenzyl_ether

    Dibenzyl ether Names Preferred IUPAC name. ... Melting point: 3.6 °C (38.5 °F; 276.8 K) Boiling point: 298 °C (568 °F; 571 K) Hazards

  3. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  4. Diphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_ether

    Diphenyl ether is the organic compound with the formula (C 6 H 5) 2 O. It is a colorless, low-melting solid. It is a colorless, low-melting solid. This, the simplest diaryl ether , has a variety of niche applications.

  5. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.

  6. Dibenzo-18-crown-6 - Wikipedia

    en.wikipedia.org/wiki/Dibenzo-18-crown-6

    Dibenzo-18-crown-6 is the organic compound with the formula [OC 6 H 4 OCH 2 CH 2 OCH 2 CH 2] 2.It is a white solid that is soluble in organic solvents. As one of the most popular crown ethers, it facilitates the dissolution of many salts in organic solvents.

  7. Para tertiary butylphenol formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Para_tertiary_butylphenol...

    Para tertiary butylphenol formaldehyde resin, also known as p-tert-butylphenol-formaldehyde resin (PTBP-FR), is a thermoplastic phenol-formaldehyde resin found in commercial adhesives, particularly glues used to bond leather and rubber.

  8. Isovaleraldehyde - Wikipedia

    en.wikipedia.org/wiki/Isovaleraldehyde

    Synthetic routes for the production of isovaleraldehyde vary. One method is by the hydroformylation of isobutene: (CH 3) 2 C=CH 2 + H 2 + CO → (CH 3) 2 CH−CH 2 CHO. A small amount of 2,2-dimethylpropanal ((CH 3) 2 C(CHO)CH 3) side product is also generated.

  9. Benzil - Wikipedia

    en.wikipedia.org/wiki/Benzil

    Benzil is a standard building block in organic synthesis.It condenses with amines to give diketimine ligands. A classic organic reaction of benzil is the benzilic acid rearrangement, in which base catalyses the conversion of benzil to benzilic acid.