28850
Cycloheptanone
purum, ≥95.0% (GC)
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About This Item
Linear Formula:
C7H12(=O)
CAS Number:
Molecular Weight:
112.17
EC Number:
207-937-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
969823
MDL number:
grade
purum
assay
≥95.0% (GC)
refractive index
n20/D 1.461
bp
179 °C (lit.)
density
0.951 g/mL at 25 °C (lit.)
SMILES string
O=C1CCCCCC1
InChI
1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2
InChI key
CGZZMOTZOONQIA-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
131.0 °F
flash_point_c
55 °C
Regulatory Information
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Richmond Sarpong et al.
Journal of the American Chemical Society, 125(45), 13624-13625 (2003-11-06)
A set of mild processes for the conversion of vinyl cyclopropyl diazo ketones to highly functionalized cycloheptadienones and vinyl cyclopentenones by use of a target-inspired tandem Wolff/Cope rearrangement sequence is described. A divergent reaction course of the vinyl cyclopropyl diazo
R Singh et al.
Current medicinal chemistry. Anti-cancer agents, 3(6), 431-438 (2003-10-08)
A series of naturally occurring and synthetic novel oxapenam (4-oxa-1-azabicyclo[3.2.0] heptan-7-one) derivatives with their antitumor activity and the structure-activity relationship among this class of compounds is reported. Among the synthetic 4-oxa-1-azabicyclo[3.2.0]heptan-7-one having an ester, amide, ether derivatives of hydroxy group
Takuya Hashimoto et al.
Journal of the American Chemical Society, 131(18), 6614-6617 (2009-04-22)
Insertion of one methylene unit into the C-C bond of cyclohexanones is a potentially useful, straightforward method for the construction of seven-membered carbocycles. An especially appealing but largely unexplored method in this arena is the nucleophilic addition of diazoalkanes to
Redouane Beniazza et al.
The Journal of organic chemistry, 76(3), 791-799 (2011-01-13)
A short access to homocalystegine analogues silylated at C7 is described. The synthesis involves the desymmetrization of a (phenyldimethylsilyl)methylcycloheptatriene using osmium-mediated dihydroxylation, followed by the diol protection and a cycloaddition involving the remaining diene moiety and an acylnitroso reagent. Additions
Khairia M Youssef et al.
Archiv der Pharmazie, 337(1), 42-54 (2004-02-05)
New series of 3, 5-bis(substituted benzylidene)-4-piperidones, 2, 7-bis(substituted benzylidene)cycloheptanones, 1, 5-bis(substituted phenyl)-1, 4-pentadien-3-ones, 1, 7-bis(substituted phenyl)-1, 6-heptadien-3, 5-diones, 1, 1-bis(substituted cinnamoyl)-cyclopentanes, and 1, 1-bis(substituted cinnamoyl)cyclohexanes have been synthesized and tested for their antioxidant activity. Among the tested compounds, compounds II(4)
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