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2,5-Cyclohexadien-1-one, 4-(2,4,6-cycloheptatrien-1-ylidene)is a chemical compound with a complex molecular structure. It is a derivative of cyclohexadienone and features a 2,4,6-cycloheptatrien-1-ylidene substituent. 2,5-Cyclohexadien-1-one, 4-(2,4,6-cycloheptatrien-1-ylidene)is used in the field of organic chemistry and has potential applications in the synthesis of various organic molecules. It may also have potential biological or pharmaceutical uses, although further research would be needed to fully understand its properties and potential applications.

1822-37-3

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1822-37-3 Usage

Uses

Used in Organic Chemistry:
2,5-Cyclohexadien-1-one, 4-(2,4,6-cycloheptatrien-1-ylidene)is used as a synthetic intermediate for the preparation of various organic molecules. Its unique structure allows for the formation of new compounds through chemical reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
Although further research is needed, 2,5-Cyclohexadien-1-one, 4-(2,4,6-cycloheptatrien-1-ylidene)may have potential applications in the pharmaceutical industry. Its complex structure could potentially be utilized in the development of new drugs or drug delivery systems, contributing to advancements in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 1822-37-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1822-37:
(6*1)+(5*8)+(4*2)+(3*2)+(2*3)+(1*7)=73
73 % 10 = 3
So 1822-37-3 is a valid CAS Registry Number.

1822-37-3Downstream Products

1822-37-3Relevant academic research and scientific papers

ELECTRONIC STRUCTURE AND KINETIC BEHAVIOR OF 4-(CYCLOHEPTATRIENYLIDENE)CYCLOHEXA-2,5-DIENONE (OR QUINAREN-9-ONE) AND ITS DERIVATIVES

Takahashi, Kazuko,Nozoe, Tetsuo,Takase, Kahei,Kudo,Toshiaki

, p. 77 - 80 (2007/10/02)

The conjugative interaction between the two terminal groups in title quinarenone 2 and its chloro- and methoxy-derivatives were evaluated, proving that the diatropicity of the seven-membered ring is a little larger in 2 than in tropone.Some of these quinarenones are also found to exist in equilibrium with their oligomers and show unexpectedly low barriers of rotation about the intercyclic bond.

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