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2-phenyl-2H-naphtho[2,3-d][1,3,2]dioxaborole is a complex organic compound characterized by a unique structure that includes a naphthalene core, a phenyl group, and a 1,3,2-dioxaborole ring system. 2-phenyl-2H-naphtho[2,3-d][1,3,2]dioxaborole is of interest in organic chemistry, particularly in the field of boron chemistry, due to its potential applications in cross-coupling reactions and as a building block for more complex molecules. The 1,3,2-dioxaborole ring is a stable and electron-rich system that can participate in various chemical transformations, making it a valuable intermediate in synthetic organic chemistry. The compound's properties, such as its reactivity and stability, are influenced by the presence of the phenyl group, which can affect its electronic and steric characteristics. Overall, 2-phenyl-2H-naphtho[2,3-d][1,3,2]dioxaborole represents an intriguing example of the diversity and complexity found in organic chemistry, with potential implications for the development of new materials and pharmaceuticals.

5785-80-8

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5785-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5785-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,8 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5785-80:
(6*5)+(5*7)+(4*8)+(3*5)+(2*8)+(1*0)=128
128 % 10 = 8
So 5785-80-8 is a valid CAS Registry Number.

5785-80-8Downstream Products

5785-80-8Relevant academic research and scientific papers

Selective isolation of polycyclic aromatic hydrocarbons by self-assembly of a tunable N→B clathrate

Herrera-Espa?a, Angel D.,Campillo-Alvarado, Gonzalo,Román-Bravo, Perla,Herrera-Ruiz, Dea,H?pfl, Herbert,Morales-Rojas, Hugo

, p. 1572 - 1576 (2015)

The combination of one dipyridyl linker [1,2-di(4-pyridyl)ethylene (DPE), 1,2-di(4-pyridyl)ethane (DPEt), or 4,4′-azopyridine (DPA)] with two molecules of arylboronate ester 1 produced dinuclear Lewis-type N→B adducts that can act as acyclic host for polycyclic aromatic hydrocarbons (PAHs) in the solid state. Nine crystalline solids of composition PAH@adduct (i.e., one PAH per adduct) were obtained from solutions containing a single PAH. On the basis of the single-crystal X-ray diffraction analysis of the compound ANT@A1 (ANT = anthracene; A1 = adduct being composed of DPE and two boronate esters 1), the PAH inclusion selectivity is related to a size-fitting adaptation to an octaedral-shaped pocket assembled by CH-π interactions between fragments of the diamine and the arylboronate ester 1. The resulting reversible organic clathrates can perform catch and release cycles of PAHs such as pyrene and can sequester selectively PAHs from mixtures in solution.

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