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1,3-Cycloheptanedione

Names

[ CAS No. ]:
1194-18-9

[ Name ]:
1,3-Cycloheptanedione

[Synonym ]:
1,3-Cycloheptanedione
Cycloheptane-1,3-dione
cyclohepta-1,3-dione
cycloheptane-1,3-quinone
1,3-cycloheptadienone
1,3-cycloheptandione
cycloheptan-1,3-dione
1,3-cycloheptadione
MFCD01863735
1,3-Dioxocycloheptane
1 3-Cycloheptanedione 97

Biological Activity

[Description]:

Cycloheptane-1,3-dione is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
250.7±23.0 °C at 760 mmHg

[ Molecular Formula ]:
C7H10O2

[ Molecular Weight ]:
126.15

[ Flash Point ]:
92.2±19.6 °C

[ Exact Mass ]:
126.068077

[ PSA ]:
34.14000

[ LogP ]:
-0.62

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.467

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2914299000

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2914299000

[ Summary ]:
2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

A Mild, Large-Scale Synthesis of 1,3-Cyclooctanedione: Expanding Access to Difluorinated Cyclooctyne for Copper-Free Click Chemistry.

Tetrahedron Lett. 52(16) , 1871-1873, (2011)

We report the large-scale synthesis of 1,3-cyclooctanedione in five steps with 29% yield. This molecule is a synthetic precurser to difluorinated cyclooctyne, which participates in a bioorthogonal cop...

Michael addition of 1, 3-cyclopentanedione, 1, 3-cyclohexanedione and 1, 3-cycloheptanedione to 1-(X-phenyl)-2-nitroethylenes. Hrnciar P and Culák I.

Collect. Czech. Chem. Commun. 49(6) , 1421-1431, (1984)

Methylation of 1, 3-cyclopentanedione, 1, 3-cyclohexanedione, and 1, 3-cycloheptanedione with iodomethane in aprotic solvents in the absence and in the presence of 18-crown-6. Šraga J and Hrnciar P.

Chemical Papers (Slovak Acad. Sci.) 35(1) , 119-126, (1981)


More Articles


Related Compounds