Skip to Content
MilliporeSigma
All Photos(1)

Documents

414522

Sigma-Aldrich

7-Oxabicyclo[4.1.0]heptan-2-one

98%

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

About This Item

Empirical Formula (Hill Notation):
C6H8O2
CAS Number:
6705-49-3
Molecular Weight:
112.13
EC Number:
229-751-4
MDL number:
MFCD00192371
UNSPSC Code:
12352100
PubChem Substance ID:
24865940
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.474 (lit.)

bp

76-78 °C/15 mmHg (lit.)

density

1.13 g/mL at 25 °C (lit.)

SMILES string

O=C1CCCC2OC12

InChI

1S/C6H8O2/c7-4-2-1-3-5-6(4)8-5/h5-6H,1-3H2

InChI key

QKOHEJBTNOEACF-UHFFFAOYSA-N

Related Categories

General description

7-Oxabicyclo[4.1.0]heptan-2-one is one of the products formed during oxidation of cyclohexene by dendritic complexes. It has been reported as anticapsin analog.

Application

7-Oxabicyclo[4.1.0]heptan-2-one was employed as substrate to investigate the substrate specificity of purified recombinant NADPH-dependent 3-quinuclidinone reductases from Microbacterium luteolum JCM 9174 for the reductive reaction of ketones.

wgk_germany

WGK 3

flash_point_f

204.8 °F

flash_point_c

96.00 °C

ppe

Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Oxidation of cyclohexene by dendritic PAMAMSA-Mn (II) complexes.
Yang Z-W, et al.
J. Mol. Catal. A: Chem., 213(2), 169-176 (2004)
Kentaro Isotani et al.
Applied and environmental microbiology, 79(4), 1378-1384 (2012-12-25)
We used the resting-cell reaction to screen approximately 200 microorganisms for biocatalysts which reduce 3-quinuclidinone to optically pure (R)-(-)-3-quinuclidinol. Microbacterium luteolum JCM 9174 was selected as the most suitable organism. The genes encoding the protein products that reduced 3-quinuclidinone were

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