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Phosphonium, (2-methoxy-9H-fluoren-9-yl)triphenyl-, bromide is a complex organic compound with the chemical formula C37H30BrO2P. It is a phosphonium salt, which is a type of onium salt that contains a phosphorus atom bonded to four other atoms or groups. In this specific compound, the phosphorus atom is bonded to three phenyl groups (C6H5) and a 2-methoxy-9H-fluoren-9-yl group. The 2-methoxy-9H-fluoren-9-yl group is a derivative of fluorene, a polycyclic aromatic hydrocarbon, with a methoxy group (-OCH3) attached to the 2-position. The compound also contains a bromide ion (Br-) as a counterion. This phosphonium salt is used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds and as a catalyst in various chemical reactions. Its unique structure and properties make it a valuable tool in the field of chemistry, particularly in the synthesis of complex organic molecules.

7293-61-0

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7293-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7293-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7293-61:
(6*7)+(5*2)+(4*9)+(3*3)+(2*6)+(1*1)=110
110 % 10 = 0
So 7293-61-0 is a valid CAS Registry Number.

7293-61-0Relevant academic research and scientific papers

A comprehensive study of substituent effects on poly(dibenzofulvene)s

Wong, Michael Y.,Leung, Louis M.

, p. 512 - 520 (2017/02/05)

We herein report the first cross comparison of 14 poly(dibenzofulvene) derivatives (13 novel examples and the parent poly(dibenzofulvene)) in order to understand how the choice of substituent affects the physical properties of this interesting class of semiconducting polymers. Electron withdrawing substituents decreased the polymerization reactivity and resulted in very low molecular-weight products. Di-substituted poly(dibenzofulvene)s were found to be much less soluble than the mono-analogues which can be explained by the Hansen solubility parameter system. Analysis based on absorption, emission and electrochemistry profiles suggests that polymer solubility is a very important factor that controls the degree of stacking present in the polymer due to synthetic issues. For the first time, the thermal analysis of the parent poly(dibenzofulvene) and its derivatives is reported and it was believed that depolymerization occurred much earlier than the melting transition. We have also demonstrated the orthogonal synthesis of dibenzofulvene monomers using three distinct routes (lithiation, oxidation and Wittig) to cope with functional group compatibility.

A facile approach to the synthesis of substituted dibenzofulvenes-precursors to pi-stacked poly(dibenzofulvene)s

Wong, Michael Y.,Leung, Louis M.

experimental part, p. 3973 - 3977 (2010/07/04)

A series of novel substituted (2-methoxy, 2-nitro, 2-bromo, 2-iodo, 2-cyano, and 2-acetyl) and disubstitiuted (2-bromo-7-methoxy, 2-bromo-7-propoxy, 2-bromo-7-hexoxy, 2-nitro-7-propoxy, 2-nitro-7-hexoxy, and 2,7-di-bromo) dibenzofulvenes have been prepared from the corresponding fluorenes with fair to very good overall yields (35.7-66.7%) based on the Wittig chemistry. The new approach enjoyed much simpler experimental procedures and has the advantage of higher functional group tolerance. Preliminary results on their polymerization using solution free-radical approach are also presented.

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