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Dimethoxymethane, also
called methylal, is a
colorless flammable liquid with a low
boiling point, low
viscosity and
excellent dissolving power. It has...
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method to
prepare chloromethyl methyl ether in situ is by
combining dimethoxymethane and
acetyl chloride,
either neat or as a
solution in an
inert solvent...
- The
molecular formula C3H8O2 may
refer to:
Dimethoxymethane 2-Methoxyethanol
Propanediol 1,2-Propanediol (propylene glycol) 1,3-Propanediol (trimethylene...
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reaction steps are equilibria.
Benzylidene acetal, a
protecting group Dimethoxymethane, a solvent, a.k.a. methylal, a.k.a.
formal [ambiguous]
Dioxolane Metaldehyde...
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Fabian (2020). "A
comprehensive kinetic model for
dimethyl ether and
dimethoxymethane oxidation and NO
interaction utilizing experimental laminar flame speed...
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original Pictet–Spengler
reaction was the
reaction of
phenethylamine and
dimethoxymethane,
catalysed by
hydrochloric acid
forming a tetrahydroisoquinoline. The...
- to
acetals CHR1(OR)2 (historical definition) and
ketals CR1R2(OR)2
Dimethoxymethane (CH2(OCH3)2) in particular, the
formal derived from
methanol A formality...
- also used in the
malonic ester synthesis. It can be
synthesized from
dimethoxymethane and
carbon monoxide. H 2 C ( O C H 3 ) 2 + 2 C O ⟶ C H 2 ( C O 2...
- alcohols,
propylene glycol, and
propylene oxide Paraform * Cyanates,
dimethoxymethane, formaldehyde, hexamethylenetetramine, paraformaldehyde, and triallylcyanurate...
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preferred for most heteroatoms,
however for the
stabilization to
occur in
dimethoxymethane, the gauche,
gauche conformation is
about 3–5 kcal/mol
lower in energy...