543179
Ethyl 2-acetoxybenzoate
98%
Synonym(s):
Ethyl acetylsalicylate
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About This Item
Linear Formula:
C6H4(OCOCH3)CO2C2H5
CAS Number:
Molecular Weight:
208.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
refractive index
n20/D 1.506 (lit.)
bp
278-279 °C (lit.)
density
1.158 g/mL at 25 °C (lit.)
functional group
ester
SMILES string
CCOC(=O)c1ccccc1OC(C)=O
InChI
1S/C11H12O4/c1-3-14-11(13)9-6-4-5-7-10(9)15-8(2)12/h4-7H,3H2,1-2H3
InChI key
UYDSGXAKLVZWIJ-UHFFFAOYSA-N
General description
Ethyl 2-acetoxybenzoate can be synthesized by reacting ethyl salicylate and acetic anhydride in the presence of zeolite Hβ. It can also be obtained from the reaction between acetylsalicyloyl chloride (in pyridine) with ethanol.
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and transdermal properties of acetylsalicylic acid and selected esters
Gerber M, et al.
International Journal of Pharmaceutics, 310.1, 31-36 (2006)
Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a solvent-free system. Scope of the reaction for substituted ethers
Smith K, et al.
Organic & Biomolecular Chemistry, 310.1, 1560-1564 (2003)
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