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  2. Sodium ethoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_ethoxide

    Melting point: 260 °C (500 °F; 533 K) Solubility in water. Reacts Solubility: ... Sodium ethoxide, also referred to as sodium ethanolate, is the ionic, ...

  3. 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.

  4. Sodium hydrosulfide - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydrosulfide

    Sodium hydrosulfide is the chemical compound ... NaSH has a relatively low melting point of 350 °C. ... One laboratory synthesis entails treatment of sodium ethoxide ...

  5. Triethyl orthoformate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_orthoformate

    It may also be prepared from the reaction of sodium ethoxide, formed in-situ from sodium and absolute ethanol, and chloroform: [2] CHCl 3 + 3 Na + 3 EtOH → HC(OEt) 3 + 3 ⁄ 2 H 2 + 3 NaCl. Triethyl orthoformate is used in the Bodroux-Chichibabin aldehyde synthesis, for example: [3] RMgBr + HC(OC 2 H 5) 3 → RC(H)(OC 2 H 5) 2 + MgBr(OC 2 H 5)

  6. Sodium methoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methoxide

    Sodium methoxide is prepared by treating methanol with sodium: 2 Na + 2 CH 3 OH → 2 CH 3 ONa + H 2. The reaction is so exothermic that ignition is possible. The resulting solution, which is colorless, is often used as a source of sodium methoxide, but the pure material can be isolated by evaporation followed by heating to remove residual methanol.

  7. List of metal-organic chemical vapour deposition precursors

    en.wikipedia.org/wiki/List_of_metal-organic...

    Melting point TG data DSC IR spectra NMR data Solubility References Li(TMHD), Lithium tetramethylheptanedionate, C 11 H 19 LiO 2: ... Sodium niobium ethoxide, NaNb(OC ...

  8. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    Sodium acetylacetonate, Na(acac), is the precursor to many acetylacetonate complexes. A general method of synthesis is to treat a metal salt with acetylacetone in the presence of a base: [12] MB z + z Hacac ⇌ M(acac) z + z BH. Both oxygen atoms bind to the metal to form a six-membered chelate ring.

  9. Sodium acetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_acetate

    Sodium acetate trihydrate crystals melt at 58–58.4 °C (136.4–137.1 °F), [12] [13] and the liquid sodium acetate dissolves in the released water of crystallization. When heated past the melting point and subsequently allowed to cool, the aqueous solution becomes supersaturated. This solution is capable of cooling to room temperature ...