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CAS No. : | 606-45-1 | MDL No. : | MFCD00008423 |
Formula : | C9H10O3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | PFYHAAAQPNMZHO-UHFFFAOYSA-N |
M.W : | 166.17 | Pubchem ID : | 61151 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
Methyl 2-methoxybenzoate (CAS: 606-45-1) can be used in the preparation of Salicylic acid (CAS: 69-72-7). Salicylic acid exhibits bacteriostatic, fungicidal, and keratolytic actions. Its salts, known as salicylates, are commonly used as analgesics.
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
66% | With molybdenum hexacarbonyl; In tetrachloromethane; at 150℃; for 6h;Autoclave; | General procedure: General procedure for the reaction of acetonitrilewith carboxylic acids. A 17-mL stainless-steelhigh-pressure microreactor was charged with 1 mmolof Mo(CO)6 or VO(acac)2, 100 mmol of carboxylicacid, 500 mmol of acetonitrile, and 50 mmol of carbontetrachloride. The reactor was hermetically closed andheated for 6 h at 150C. When the reaction wascomplete, the reactor was cooled to room temperatureand opened, the mixture was filtered through a layer ofAl2O3, unreacted acetonitrile and carbon tetrachloridewere distilled off, and the residue was distilled underatmospheric or reduced pressure or recrystallized fromethanol. |
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