297852
Ethyl p-tolylacetate
98%
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About This Item
Linear Formula:
CH3C6H4CH2CO2C2H5
CAS Number:
Molecular Weight:
178.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
237-904-1
Beilstein/REAXYS Number:
2045927
MDL number:
Assay:
98%
assay
98%
SMILES string
CCOC(=O)Cc1ccc(C)cc1
InChI key
BTRGZBIXPLFVNK-UHFFFAOYSA-N
InChI
1S/C11H14O2/c1-3-13-11(12)8-10-6-4-9(2)5-7-10/h4-7H,3,8H2,1-2H3
Quality Level
bp
116-118 °C/13 mmHg (lit.)
density
1.008 g/mL at 25 °C (lit.)
functional group
ester
Related Categories
Application
Ethyl p-tolylacetate was used in preparation of:
- ethyl-substituted phenylpropioloylacetates
- ethyl 2-(4-bromomethylphenyl)propionate
- (−)-incrustoporin, antifungal agent
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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The condensation of acetylenic esters with ethyl phenylacetates.
Al-Jallo HN and Al-Hajjar FH.
J. Chem. Soc. Sect. C, 15, 2056-2058 (1970)
Synthesis of 2-(4-bromomethylphenyl) propionic acid and ester.
Liu Z-X and Cheng Q-R.
Chemical Reagents, 4, 021-021 (2011)
Ring-Closing Metathesis Enabled Efficient Synthesis of ?-Butenolide Antifungal Agent (-)-Incrustoporin and its Analogues.
Fernandes RA, et al.
Asian Journal of Organic Chemistry, 3(1), 58-62 (2014)
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