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C120006

Sigma-Aldrich

Cyclopropyl methyl ketone

99%

Synonym(s):

Acetylcyclopropane

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About This Item

Linear Formula:
C3H5COCH3
CAS Number:
Molecular Weight:
84.12
Beilstein/REAXYS Number:
1633817
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

liquid

refractive index

n20/D 1.424 (lit.)

bp

114 °C (lit.)

density

0.849 g/mL at 25 °C (lit.)

SMILES string

CC(=O)C1CC1

InChI

1S/C5H8O/c1-4(6)5-2-3-5/h5H,2-3H2,1H3

InChI key

HVCFCNAITDHQFX-UHFFFAOYSA-N

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Application

  • Synthesis of 1,2,4-trioxepanes and 1,2,4-trioxocanes via photooxygenation of homoallylic alcohols.: This study explores the synthesis of novel 1,2,4-trioxepanes and 1,2,4-trioxocanes through the photooxygenation of homoallylic alcohols, utilizing Cyclopropyl methyl ketone as a key reagent in the process. The findings highlight the efficiency and potential applications of this synthetic pathway in organic chemistry and pharmaceutical intermediate production (Singh et al., 2006).

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1C

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

69.8 °F - closed cup

flash_point_c

21 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

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Shigeo Hayashi et al.
Journal of enzyme inhibition and medicinal chemistry, 29(6), 846-867 (2014-02-13)
Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatment of inflammatory diseases/syndromes; however, traditional NSAIDs exhibit serious side-effects such as gastrointestinal damage

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