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1573202-44-4

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1573202-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1573202-44-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,3,2,0 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1573202-44:
(9*1)+(8*5)+(7*7)+(6*3)+(5*2)+(4*0)+(3*2)+(2*4)+(1*4)=144
144 % 10 = 4
So 1573202-44-4 is a valid CAS Registry Number.

1573202-44-4Downstream Products

1573202-44-4Relevant articles and documents

Carbohydrate double-nitrogen heterocyclic carbene precursor salt and its preparation and use (by machine translation)

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Paragraph 0047-0050, (2018/03/24)

The present invention provides a carbohydrate double-nitrogen heterocyclic carbene precursor salt and its preparation and use, the structure shown in formula I: The invention through the cheap and easy to obtain, three-dimensional chemical rich monosaccharide as a chiral source of chiral catalyst, for two different synthesis method carbohydrate double-nitrogen heterocyclic carbene precursor salt, as a palladium-catalyzed Buchwald - Hartwig reaction catalyst, replacing the toxicity, extremely sensitive to water and oxygen phosphine, synthesis has the value of the practical application of the Spiro - OMeTAD and its derivatives, overcome the preparation Spiro - OMeTAD and its derivatives of complex steps, a plurality of product components, not easy purification, low yield and the like. (by machine translation)

NEW SPIRO COMPOUNDS AND THEIR USE IN ORGANIC ELECTRONICS APPLICATIONS AND DEVICES

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Paragraph 0184; 0194-0195, (2016/12/26)

The present invention relates 9,9'-spirobifluorene compounds of general formula (I) wherein the variables R11, R12, R21, R22, R31, R32, R41 and R42 independently of each other have the meaning of aryl or hetaryl, with the proviso that not all of the radicals R11, R12, R21, R22, R31, R32, R41 and R42 are identical, to the use of compounds of general formula I in organic electronics applications, especially in organic field effect transistors, in organic photodetectors and organic solar cells, specifically in dye-sensitized solar cells and bulk heterojunction solar cells, and to an organic field effect transistor, a dye-sensitized solar cell and a bulk heterojunction solar cell comprising compounds of general formula I.

O-methoxy substituents in spiro-OMeTAD for efficient inorganic-organic hybrid perovskite solar cells

Jeon, Nam Joong,Lee, Hag Geun,Kim, Young Chan,Seo, Jangwon,Noh, Jun Hong,Lee, Jaemin,Seok, Sang Il

supporting information, p. 7837 - 7840 (2014/06/23)

Three spiro-OMeTAD derivatives have been synthesized and characterized by 1H/13C NMR spectroscopy and mass spectrometry. The optical and electronic properties of the derivatives were modified by changing the positions of the two methoxy substituents in each of the quadrants, as monitored by UV-vis spectroscopy and cyclic voltammetry measurements. The derivatives were employed as hole-transporting materials (HTMs), and their performances were compared for the fabrication of mesoporous TiO2/CH 3NH3PbI3/HTM/Au solar cells. Surprisingly, the cell performance was dependent on the positions of the OMe substituents. The derivative with o-OMe substituents showed highly improved performance by exhibiting a short-circuit current density of 21.2 mA/cm2, an open-circuit voltage of 1.02 V, and a fill factor of 77.6% under 1 sun illumination (100 mW/cm2), which resulted in an overall power conversion efficiency (PCE) of 16.7%, compared to ~15% for conventional p-OMe substituents. The PCE of 16.7% is the highest value reported to date for perovskite-based solar cells with spiro-OMeTAD.

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