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637-88-7 - 1,4-Cyclohexanedione, 98% - A11100 - Alfa Aesar

A11100 1,4-Cyclohexanedione, 98%

CAS Number
637-88-7
Synonyms

Size Price ($) Quantity Availability
25g 48.93
100g 124.11
500g 440.00
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1,4-Cyclohexanedione, 98%

MDL
MFCD00001606
EINECS
211-306-0

Chemical Properties

Formula
C6H8O2
Formula Weight
112.13
Melting point
77-78°
Boiling Point
132°/20mm
Flash Point
132°(269°F)
Solubility
Soluble in methanol and ethanol.

Applications

1,4-Cyclohexanedione is used in the preparation of 1,4 benzoquinone and bromoorganics. It is also used to study the influence of visible light on the bromate-1,4-cyclohexanedione-ferroin oscillating reaction. It plays a vital role in pharmaceuticals, plant growth regulator and as a conducting material.

Notes

Incompatible with strong oxidizing agents.

Literature References

Miyazato, H.; Nakamura, M.; Hashimoto, S.; Hayashi, S. Identification of the odour-active cyclic diketone cis-2,6-dimethyl-1,4-cyclohexanedione in roasted Arabica coffee brew. Food Chem. 2013, 138(4), 2346-2355.

Li, J.; Wang, J. Complex Dynamical Behavior in the Highly Photosensitive Cerium-Bromate-1,4-Benzoquinone Reaction. J. Phys. Chem. A 2012, 116 (31), 8130-8137.

Chen, Z.; Yang, W.; Hu, Y-H.; Lei, Z-Y.; Wang, Y-H.; Wan, W-Q. Measurement and Correlation for the Solubility of Dimethyl 1,4-Cyclohexanedione-2,5-dicarboxylate in Different Solvents at Temperatures from (278.15 to 323.15) K. J. Chem. Eng. Data 2011, 56 (5), 2726-2729.

Bell, J. G.; Wang, J. Complex Spatiotemporal Behavior in the Photosensitive Ferroin-Bromate-4-Nitrophenol Reaction. J. Phys. Chem. A 2015, 119 (14), 3323-3328.

Budroni, M. A.; Rossi, F. A Novel Mechanism for in Situ Nucleation of Spirals Controlled by the Interplay between Phase Fronts and Reaction-Diffusion Waves in an Oscillatory Medium. J. Phys. Chem. C 2015, 119 (17), 9411-9417.

Other References

Beilstein
774152
Harmonized Tariff Code
2914.29
TSCA
Yes

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