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514691

Sigma-Aldrich

Ethyl 4-cyanobenzoylformate

95%

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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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCF8963
MKCB9317
MKBN4104V
MKBD7345
01422AJ

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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

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