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Naphthalene, 2,2-(1,2-ethenediyl)bis-, also known as 1,2-bis(naphthalen-2-yl)ethene or di(2-naphthyl)ethylene, is an organic compound with the chemical formula C24H18. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. Naphthalene, 2,2- (1,2-ethenediyl)bis- is formed by the linkage of two naphthalene molecules through an ethylene bridge, resulting in a planar structure. It is used in the synthesis of various organic compounds and as a precursor in the production of polymers and pharmaceuticals. Due to its aromatic nature, it exhibits certain optical and electronic properties, making it a subject of interest in materials science and chemistry.

2042-99-1

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2042-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2042-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,4 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2042-99:
(6*2)+(5*0)+(4*4)+(3*2)+(2*9)+(1*9)=61
61 % 10 = 1
So 2042-99-1 is a valid CAS Registry Number.

2042-99-1Relevant academic research and scientific papers

Model Guided Development of a Simple Catalytic Method for the Synthesis of Unsymmetrical Stilbenes by Sequential Heck Reactions of Aryl Bromides with Ethylene

Barlow, Helen,Buser, Jonas Y.,Glauninger, Hendrik,Luciani, Carla V.,Martinelli, Joseph R.,Oram, Niall,Thompson-Van Hook, Nichole,Richardson, Jeffery

supporting information, p. 2678 - 2690 (2018/06/04)

Stilbenes are important and useful structural moieties, but methods for their preparation typically possess numerous inefficiencies. Presented here is a methodology for the two-step, one pot preparation of unsymmetrical stilbenes via sequential Heck reactions. The first Heck reaction with ethylene gas was analysed as a function of temperature and pressure for electronically differentiated naphthyl bromides and model-aided reaction optimization was utilized to define the system. In addition, reactNMR was utilized to determine ethylene solubility in common organic solvents useful for Heck reactions. Finally, an optimized sequential Heck reaction process was developed and applied to a range of substrates allowing for efficient preparation of unsymmetrical stilbenes, including the natural antioxidant, pterostilbene. (Figure presented.).

PHASE TRANSFER CATALYSED POLYMER-SUPPORTED WITTIG REACTIONS

Clarke, Stephen D.,Harrison, Charles R.,Hodge, Philip

, p. 1375 - 1378 (2007/10/02)

Arylsubstituted olefins can be prepared in high yield using phase transfer catalysed polymer-supported Wittig reactions.

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