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1-Tert-butyl-cyclopenten-(1)-dion-(3,5) is a complex organic compound with the molecular formula C9H12O2. It features a cyclopentenone ring, which is a five-membered ring with one double bond and one ketone group, and a tert-butyl group attached to the first carbon. The compound is characterized by its unique structure, which includes a cycloalkane ring and a ketone functional group, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its stability and reactivity can be influenced by the presence of the tert-butyl group, which provides steric hindrance and can affect the compound's chemical properties and potential applications in organic synthesis.

3790-93-0

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3790-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3790-93-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3790-93:
(6*3)+(5*7)+(4*9)+(3*0)+(2*9)+(1*3)=110
110 % 10 = 0
So 3790-93-0 is a valid CAS Registry Number.

3790-93-0Upstream product

3790-93-0Downstream Products

3790-93-0Relevant academic research and scientific papers

Extradiol Oxygenation of 3,5-Di-tert-butylcatechol with O2 by Iron Chlorides in Tetrahydrofuran-Water as a Model Reaction for Catechol-2,3-dioxygenases

Funabiki, Takuzo,Yoneda, Izumi,Ishikawa, Michiya,Ujiie, Mikio,Nagai, Yasutaka,Yoshida, Satohiro

, p. 1453 - 1454 (1994)

Selective extradiol oxygenation of 3,5-di-tert-butylcatechol 1 with O2 catalysed by Fe2+ is achieved in THF in the presence of water; the different selectivity obtained by FeCl2 and FeCl3 in THF-H2O and THF-pyridine supports the explanation of the intra- and extra-diol oxygenations by Fe3+ and Fe2+, respectively, as proposed in the enzymatic systems.

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