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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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 Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
203.0 °F - closed cup
Flash Point(C)
95 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Intracanal medication in endodontic treatment: a survey of endodontic programs.
J M Gergely et al.
General dentistry, 41(4), 328-331 (1993-07-01)
P Ohara et al.
Journal of endodontics, 19(10), 498-500 (1993-10-01)
This study was undertaken to determine the antibacterial effects of various endodontic medicaments against six selected anaerobic bacteria. The experiment involved the testing of the vapors of six medicaments using agar plates streaked with the bacteria. A zone of inhibition
[Basic studies on the clinical application of cresatin].
K Miyazawa
Shigaku = Odontology; journal of Nihon Dental College, 70(6), 1268-1279 (1983-04-01)
Systemic effects of endodontic intracanal medicaments, irrigants and sealers: danger on the bracket table.
D R Morse et al.
Annals of dentistry, 44(1), 6-15 (1985-01-01)
P M DiFiore et al.
Oral surgery, oral medicine, and oral pathology, 55(1), 91-94 (1983-01-01)
Four calcium hydroxide-based apexification pastes were tested for their antibacterial effects on Streptococcus sanguis. Their zones of growth inhibition on blood agar plates were measured at 2, 4, 6, and 8 days. Only the camphorated parachlorophenol and the metacresylacetate pastes
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