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About This Item
Linear Formula:
C6H5COC4H7
CAS Number:
Molecular Weight:
160.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
refractive index
n20/D 1.547 (lit.)
bp
114-118 °C/7 mmHg (lit.)
density
1.05 g/mL at 25 °C (lit.)
SMILES string
O=C(C1CCC1)c2ccccc2
InChI
1S/C11H12O/c12-11(10-7-4-8-10)9-5-2-1-3-6-9/h1-3,5-6,10H,4,7-8H2
InChI key
MVEBDOSCXOQNAR-UHFFFAOYSA-N
General description
Cyclobutyl phenyl ketone reacts with 2-butanol and di-t-butyl peroxide to yield valerophenone.
Application
Cyclobutyl phenyl ketone was used to study thermal reactions of parent and phenyl substituted N-acyl cyclobutylimines.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), 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’.
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Find documentation for the products that you have recently purchased in the Document Library.
Some Reactions of Cyclobutylcarbinyl Radical Intermediates.
Neckers DC, et al.
The Journal of Organic Chemistry, 31(2), 622-624 (1966)
Thermal Reactions of N-Acyl Phenylcyclobutylimines.
Wu PL.
J. Chin. Chem. Soc., 45, 183-188 (1998)
Jose Serrano et al.
Xenobiotica; the fate of foreign compounds in biological systems, 50(2), 192-208 (2019-03-20)
1. Cyclic phenones are chemicals of interest to the USEPA due to their potential for endocrine disruption to aquatic and terrestrial species.2. Prior to this report, there was very limited information addressing metabolism of cyclic phenones by fish species and
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