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414522

Sigma-Aldrich

7-Oxabicyclo[4.1.0]heptan-2-one

98%

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5 G
¥23,500

¥23,500

Estimated to ship onApril 13, 2025

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5 G
¥23,500

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

¥23,500

Estimated to ship onApril 13, 2025

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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.)

functional group

ether
ketone

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

General description

7-Oxabicyclo[4.1.0]heptan-2-one is one of the products formed during oxidation of cyclohexene by dendritic complexes.[1] It has been reported as anticapsin analog.[2]

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.[2]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

204.8 °F - closed cup

Flash Point(C)

96.00 °C - closed cup

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.

FSL

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

JAN Code

414522-BULK:
414522-1G:
414522-VAR:
414522-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
0000237100
0000228741
0000210295
0000199825
MKCC4051

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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
Oxidation of cyclohexene by dendritic PAMAMSA-Mn (II) complexes.
Yang Z-W, et al.
J. Mol. Catal. A: Chem., 213(2), 169-176 (2004)

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