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1,3-Cyclohexanedione, 2,2'-(2-methylpropylidene)bis[5,5-dimethyl- is a complex organic compound with the chemical formula C17H26O4. It is a white crystalline solid that is soluble in organic solvents. 1,3-Cyclohexanedione, 2,2'-(2-methylpropylidene)bis[5,5-dimethyl- is characterized by a cyclohexane ring with two carbonyl groups at the 1 and 3 positions, and two 5,5-dimethyl-2,2'-cyclohexanedione units connected by a 2-methylpropylidene bridge. It is used in the synthesis of various chemicals and as an intermediate in the production of certain pharmaceuticals and polymers. Due to its complex structure, it is important in the field of organic chemistry and has potential applications in the development of new materials and compounds.

3316-12-9

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3316-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3316-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3316-12:
(6*3)+(5*3)+(4*1)+(3*6)+(2*1)+(1*2)=59
59 % 10 = 9
So 3316-12-9 is a valid CAS Registry Number.

3316-12-9Downstream Products

3316-12-9Relevant academic research and scientific papers

Merging supramolecular catalysis and aminocatalysis: Amino-appended β-cyclodextrins (ACDs) as efficient and recyclable supramolecular catalysts for the synthesis of tetraketones

Ren, Yufeng,Yang, Bo,Liao, Xiali

, p. 22034 - 22042 (2016/03/08)

Well-designed amino-appended β-cyclodextrins (ACDs) with an amino side chain of different lengths at the primary face of β-CD were synthesized and employed in the catalytic synthesis of a series of tetraketones as supramolecular catalysts in water for the first time. Yields of 58-97% were obtained with up to 30 examples of substrate. The catalyst could be recycled easily, while a 92% yield and 84% rate of catalyst recovery could be achieved after 8 cycles of catalyst recycling. Moreover, a catalytic mechanism merging supramolecular catalysis and aminocatalysis could be proposed through detailed 1D and 2D NMR, ESI-MS and Job plot analyses. This protocol retained the promising characteristics of ambient temperature, green medium, simple operation, broad substrate scope, excellent yields, superb catalyst recycling performance and unique catalytic mechanism.

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