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297852

Sigma-Aldrich

Ethyl p-tolylacetate

98%

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About This Item

Linear Formula:
CH3C6H4CH2CO2C2H5
CAS Number:
14062-19-2
Molecular Weight:
178.23
Beilstein:
2045927
EC Number:
237-904-1
MDL number:
MFCD00009181
UNSPSC Code:
12352100
PubChem Substance ID:
24857933
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.496 (lit.)

bp

116-118 °C/13 mmHg (lit.)

density

1.008 g/mL at 25 °C (lit.)

functional group

ester

SMILES string

CCOC(=O)Cc1ccc(C)cc1

InChI

1S/C11H14O2/c1-3-13-11(12)8-10-6-4-9(2)5-7-10/h4-7H,3,8H2,1-2H3

InChI key

BTRGZBIXPLFVNK-UHFFFAOYSA-N

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Application

Ethyl p-tolylacetate was used in preparation of:
  • ethyl-substituted phenylpropioloylacetates
  • ethyl 2-(4-bromomethylphenyl)propionate
  • (−)-incrustoporin, antifungal agent

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW4595
MKCR9277
S64291V
MKBD1590
20896LJ

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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)
The condensation of acetylenic esters with ethyl phenylacetates.
Al-Jallo HN and Al-Hajjar FH.
J. Chem. Soc. Sect. C, 15, 2056-2058 (1970)

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