531677
m-Tolyl acetate
97%
Synonym(s):
3-Methylphenylacetate, m-Cresyl acetate, Acetic acid m-tolyl ester
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About This Item
Linear Formula:
CH3C6H4OCOCH3
CAS Number:
Molecular Weight:
150.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
97%
refractive index
n20/D 1.501 (lit.)
bp
210-213 °C (lit.)
density
1.04 g/mL at 25 °C (lit.)
functional group
ester
SMILES string
CC(=O)Oc1cccc(C)c1
InChI
1S/C9H10O2/c1-7-4-3-5-9(6-7)11-8(2)10/h3-6H,1-2H3
InChI key
OTGAHJPFNKQGAE-UHFFFAOYSA-N
General description
m-Tolyl acetate is an acyloxy benzene derivative that can be prepared from m-cresol and acetic anhydride.
Application
m-Tolyl acetate may be used in the preparation of 2-hydroxy-4-methylacetophenone and 4-hydroxy-2-methyl acetophenone via Fries rearrangement.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
203.0 °F - closed cup
flash_point_c
95 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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J M Gergely et al.
General dentistry, 41(4), 328-331 (1993-07-01)
[Basic studies on the clinical application of cresatin].
K Miyazawa
Shigaku = Odontology; journal of Nihon Dental College, 70(6), 1268-1279 (1983-04-01)
Effect of ketoconazole on external otitis.
K Gintautiene et al.
Proceedings of the Western Pharmacology Society, 34, 351-352 (1991-01-01)
Synthesis and characterization of o-hydroxyarylalkylketones by using eco-friendly solvent free catalyst in frie's rearrangement.
Chouke PB and Vishwas NI.
Der Pharma Chemica, 4(1), 377-382 (2012)
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D R Morse et al.
Annals of dentistry, 44(1), 6-15 (1985-01-01)
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