Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

514691

Sigma-Aldrich

Ethyl 4-cyanobenzoylformate

95%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
NCC6H4COCO2C2H5
CAS Number:
302912-31-8
Molecular Weight:
203.19
MDL number:
MFCD01319614
UNSPSC Code:
12352100
PubChem Substance ID:
24873768
NACRES:
NA.22

Quality Level

100

Assay

95%

refractive index

n20/D 1.537 (lit.)

bp

313 °C (lit.)

density

1.18 g/mL at 25 °C (lit.)

functional group

ester
ketone
nitrile

SMILES string

CCOC(=O)C(=O)c1ccc(cc1)C#N

InChI

1S/C11H9NO3/c1-2-15-11(14)10(13)9-5-3-8(7-12)4-6-9/h3-6H,2H2,1H3

InChI key

MGBZXMQPYAYPIQ-UHFFFAOYSA-N

Related Categories

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

514691-5G:4548173164816
514691-BULK:
514691-VAR:
514691-1G:4548173164809

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCF8963
MKCB9317
MKBN4104V
MKBD7345
01422AJ

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

Regina Kratzer et al.
Microbial cell factories, 7, 37-37 (2008-12-17)
Whole cell-catalyzed biotransformation is a clear process option for the production of chiral alcohols via enantioselective reduction of precursor ketones. A wide variety of synthetically useful reductases are expressed heterologously in Escherichia coli to a high level of activity. Therefore
Christoph Gruber et al.
Biotechnology journal, 8(6), 699-708 (2013-04-17)
Generally, recombinant and native microorganisms can be employed as whole-cell catalysts. The application of native hosts, however, shortens the process development time by avoiding multiple steps of strain construction. Herein, we studied the NAD(P)H-dependent reduction of o-chloroacetophenone by isolated xylose

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