514691
Ethyl 4-cyanobenzoylformate
95%
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About This Item
Linear Formula:
NCC6H4COCO2C2H5
CAS Number:
Molecular Weight:
203.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
Ethyl 4-cyanobenzoylformate, 95%
InChI
1S/C11H9NO3/c1-2-15-11(14)10(13)9-5-3-8(7-12)4-6-9/h3-6H,2H2,1H3
SMILES string
CCOC(=O)C(=O)c1ccc(cc1)C#N
InChI key
MGBZXMQPYAYPIQ-UHFFFAOYSA-N
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
Quality Level
Related Categories
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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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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