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Merck

262536

Sigma-Aldrich

trans-3-Nonen-2-one

95%

Sinónimos:

(3E)-3-Nonen-2-one, (3E)-Non-3-en-2-one, (E)-3-Nonen-2-one

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About This Item

Fórmula lineal:
CH3(CH2)4CH=CHCOCH3
Número de CAS:
Peso molecular:
140.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

95%

refractive index

n20/D 1.449 (lit.)

bp

85 °C/12 mmHg (lit.)

density

0.848 g/mL at 25 °C (lit.)

functional group

ketone

SMILES string

[H]\C(CCCCC)=C(\[H])C(C)=O

InChI

1S/C9H16O/c1-3-4-5-6-7-8-9(2)10/h7-8H,3-6H2,1-2H3/b8-7+

InChI key

HDKLIZDXVUCLHQ-BQYQJAHWSA-N

Application

trans-3-Nonen-2-one has been used:
  • as substrate to investigate steady-state kinetics of NADPH oxidation
  • in the preparation of azido quinolone

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

179.6 °F - closed cup

flash_point_c

82 °C - closed cup

ppe

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


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Ryan A Dick et al.
The Journal of biological chemistry, 279(17), 17269-17277 (2004-02-18)
NADPH-dependent alkenal/one oxidoreductase (AOR) from the rat is a phase 2/antioxidative enzyme that is known to catalyze the reduction of the carbon-carbon double bond of alpha,beta-unsaturated aldehydes and ketones. It is also known for its leukotriene B(4) 12-hydroxydehydrogenase activity. In
Hajoong Lee et al.
The Journal of organic chemistry, 75(5), 1756-1759 (2010-02-10)
We describe the assembly of a 960-member library of tricyclic 2,3-dihydro-4-quinolones using a combination of solution-phase high-throughput organic synthesis and parallel chromatographic purification. The library was produced with high efficiency and complete chemo- and diastereoselectivity by diversification of an azide-bearing
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