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Methyl methanoate

Synonyms AI3-00408 BRN 1734623 Caswell No. 570 CCRIS 6062 EINECS 203-481-7 EPA pesticide chemical code 053701 Formic acid, methyl ester Methanoic acid, methyl ester Methyl methanoate UN 1243. [Pg.759]

Methyl methacrylate monomer, see Methyl methacrylate IV-Methylmethanamine, see Dimethylamine Methyl methanoate, see Methyl formate Methyl-a-methylacrylate, see Methyl methacrylate Methyl-2-methyl-2-propenoate, see Methyl methacrylate Methyl 2-methyl-l-propenyl ketone, see Mesityl oxide p-Methylnaphthalene, see 2-Methylnaphthalene IV-Methyl-l-naphthylcarbamate, see Carbaryl IV-Methyl-a-naphthylcarbamate, see Carbaryl IV-Methyl-a-naphthylurethan, see Carbaryl... [Pg.1495]

Synonyms Methyl methanoate formic acid, methyl ester... [Pg.479]

Comparison of the CD-spectra of (—)(R)-2-methyl-methano[10]anulene 100)117) and of (—)-8-methyl-methano[10]azaanulene 108) 1221 allowed a rather tentative assignment of the descriptor R) to -)-108 and — on the basis of the above-mentioned correlation — also to (—)-107 and to other levorotatory [10]azaanulenes, as shown in the following ... [Pg.52]

Synonym formic acid methyl ester, methyl methanoate... [Pg.773]

F.l) (FA) Formic acid, methyl ester, methyl formate, methyl methanoate 107-31-3]... [Pg.170]

METHYL METHANOATE (107-31-3) Forms explosive mixture with air (flash point —25°F/—32°C). Reacts with water, causing slow decomposition. Reacts violently with strong oxidizers. Incompatible with strong acids, alkalis, nitrates. Attacks some plastics and coatings. Flow or agitation of substance may generate electrostatic charges due to low conductivity. [Pg.790]

SYNONYMS formic acid methyl ester, methanoic acid methyl ester, methyl ester of formic acid, methyl methanoate. [Pg.746]

Synonyms/Trade Names Methyl ester of formic acid, Methyl methanoate ... [Pg.210]

Methyl methanoate. See Methyl formate Methyl methansulfonate. See Methyl methanesulfonate... [Pg.2654]

Metallic components have also been added to a variety of heterogeneous oxide catalysts, to introduce additional hydrogenation, dehydrogenation and hydrogen transfer processes during aldolization, ketonization or Tishchenko reactions. Examples include acetone (propanone) to 4-methyl-pentan-2-one, ethanol to acetone and methanol to methyl formate (methyl methanoate), e.g. [Pg.337]

See other pages where Methyl methanoate is mentioned: [Pg.319]    [Pg.228]    [Pg.42]    [Pg.354]    [Pg.2112]    [Pg.312]    [Pg.193]    [Pg.57]    [Pg.926]    [Pg.1776]    [Pg.326]    [Pg.326]    [Pg.351]    [Pg.312]    [Pg.2029]    [Pg.20]    [Pg.155]    [Pg.172]    [Pg.716]    [Pg.947]    [Pg.933]    [Pg.76]    [Pg.33]    [Pg.989]    [Pg.138]    [Pg.139]    [Pg.449]    [Pg.1010]    [Pg.1035]    [Pg.44]    [Pg.378]    [Pg.431]    [Pg.11]   
See also in sourсe #XX -- [ Pg.479 ]

See also in sourсe #XX -- [ Pg.210 ]



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