Skip to Content
Merck
CN

689963

Ethyl benzoylacetate

Arxada quality, ≥98% (GC)

Synonym(s):

Benzoylacetic acid ethyl ester, Ethyl 3-oxo-3-phenylpropionate

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C6H5COCH2COOC2H5
CAS Number:
94-02-0
Molecular Weight:
192.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329761302
EC Number:
202-295-3
Beilstein/REAXYS Number:
389944
MDL number:
MFCD00009196
Assay:
≥98% (GC)
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Ethyl benzoylacetate, Arxada quality, ≥98% (GC)

InChI

1S/C11H12O3/c1-2-14-11(13)8-10(12)9-6-4-3-5-7-9/h3-7H,2,8H2,1H3

InChI key

GKKZMYDNDDMXSE-UHFFFAOYSA-N

SMILES string

CCOC(=O)CC(=O)c1ccccc1

vapor density

6.6 (vs air)

assay

≥98% (GC)

form

liquid

quality

Arxada quality

manufacturer/tradename

Arxada AG

refractive index

n20/D 1.52 (lit.)

bp

265-270 °C (lit.)

density

1.11 g/mL at 25 °C (lit.)

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Ethyl benzoylacetate is a general reagent used in the synthesis of substituted pyrroles, oxazoles, indoles, imidazo[1, 2-a] pyridines and a variety of other aromatic compounds.

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

284.0 °F - closed cup

flash_point_c

140 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCB3552
BCCM9055
BCCH1317
BCBZ6330
BCBR5553V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Expedient synthesis of highly substituted pyrroles via tandem rearrangement of α-diazo oxime ethers.
Jiang Y, et al.
Journal of the American Chemical Society, 134(9), 4104-4107 (2012)
Rhenium-and manganese-catalyzed synthesis of aromatic compounds from 1, 3-dicarbonyl compounds and alkynes.
Kuninobu Y, et al.
The Journal of Organic Chemistry, 75(2), 334-341 (2009)
Facile synthesis of polysubstituted oxazoles via a copper-catalyzed tandem oxidative cyclization.
Wan C, et al.
Organic Letters, 12(10), 2338-2341 (2010)
Facile access to polysubstituted indoles via a cascade Cu-catalyzed arylation? condensation process.
Chen Y, et al.
The Journal of Organic Chemistry, 72(24), 9329-9334 (2007)
TBAI-catalyzed oxidative coupling of aminopyridines with β-keto esters and 1, 3-diones?synthesis of imidazo [1, 2-a] pyridines.
Ma L, et al.
Chemical Communications (Cambridge, England), 47(40), 11333-11335 (2011)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service