Methyl formate - Wikipedia
Methyl formate, also called methyl methanoate, is the methyl ester of formic acid. The simplest example of a carboxylate ester, it is a colorless liquid with an ethereal odour, high vapor pressure, and low surface tension. It is a precursor to many other compounds of commercial interest. [4]
Formate - Wikipedia
The most important formate ester is methyl formate, which is produced as an intermediate en route to formic acid. Methanol and carbon monoxide react in the presence of a strong base, such as sodium methoxide: [1] CH 3 OH + CO → HCOOCH 3. Hydrolysis of methyl formate gives formic acid and regenerates methanol: HCOOCH 3 → HCOOH + CH 3 OH
5.6: Esters - Structures and Names - Chemistry LibreTexts
2021年7月14日 · The esters shown here are ethyl acetate (a) and methyl butyrate (b). Esters occur widely in nature. Unlike carboxylic acids, esters generally have pleasant odors and are often responsible for the characteristic fragrances of fruits and flowers.
Methyl formate - NIST Chemistry WebBook
Formula: C 2 H 4 O 2. Molecular weight: 60.0520. IUPAC Standard InChI:InChI=1S/C2H4O2/c1-4-2-3/h2H,1H3 Copy. IUPAC Standard InChIKey:TZIHFWKZFHZASV-UHFFFAOYSA-N Copy. CAS Registry Number: 107-31-3.
9.8: Esters: Structures and Names - Chemistry LibreTexts
Esters feature a carbon-to-oxygen double bond that is also singly bonded to a second oxygen atom, which is then joined to an alkyl or an aryl group. The esters shown here are ethyl acetate (a) and methyl butyrate (b). Esters occur widely in nature.
Methyl formate | HCOOCH3 | CID 7865 - PubChem
Methyl formate is a formate ester resulting from the formal condensation of formic acid with methanol. A low-boiling (31.5 ℃) colourless, flammable liquid, it has been used as a fumigant and larvicide for tobacco and food crops.
Methyl Formate - Purdue University
Learn about the properties and uses of methyl formate, a simple ester with a fruity odor, from Purdue University's chemistry experts.