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1-(tert-butyl)-4-(3-methylbut-3-en-1-yl)benzene is an organic compound with the molecular formula C15H24. It is a derivative of benzene, featuring a tert-butyl group attached to the first carbon atom and a 3-methylbut-3-en-1-yl group attached to the fourth carbon atom. The presence of the 3-methylbut-3-en-1-yl group introduces a double bond, making it an unsaturated hydrocarbon. 1-(tert-butyl)-4-(3-methylbut-3-en-1-yl)benzene is characterized by its unique structure, which combines the stability of the tert-butyl group with the reactivity of the alkenyl group. It is a colorless liquid with a distinctive aromatic odor and is used in various chemical reactions and as an intermediate in the synthesis of more complex organic compounds.

3605-32-1

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3605-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3605-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3605-32:
(6*3)+(5*6)+(4*0)+(3*5)+(2*3)+(1*2)=71
71 % 10 = 1
So 3605-32-1 is a valid CAS Registry Number.

3605-32-1Downstream Products

3605-32-1Relevant academic research and scientific papers

Phosphorus Coordination Chemistry in Catalysis: Air Stable P(III)-Dications as Lewis Acid Catalysts for the Allylation of C-F Bonds

Chitnis, Saurabh S.,Lafortune, James H. W.,Cummings, Haley,Liu, Liu Leo,Andrews, Ryan,Stephan, Douglas W.

, p. 4540 - 4544 (2018)

Modification of C-F bonds with main-group catalysts has typically employed electron-deficient Lewis superacids in high oxidation states, and the challenges of preparing and handling such species have prevented broader adoption of metal-free reduction protocols. Here, we show that a hemilabile ligand coordinated to an easily accessed P(III) center imparts air stability without sacrificing the ability to activate C-F bonds. Catalytic C-C coupling of benzyl fluorides with allylsilanes was achieved using a P(III) complex under benchtop conditions. This application of coordination chemistry principles to main-group Lewis acids reveals a new strategy for controlling catalysis.

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