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960067-92-9

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960067-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960067-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,0,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 960067-92:
(8*9)+(7*6)+(6*0)+(5*0)+(4*6)+(3*7)+(2*9)+(1*2)=179
179 % 10 = 9
So 960067-92-9 is a valid CAS Registry Number.

960067-92-9Downstream Products

960067-92-9Relevant articles and documents

ORGANOMETALLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME, AND DIAGNOSTIC COMPOSITION INCLUDING THE ORGANOMETALLIC COMPOUND

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Paragraph 0320-0322; 0342-0343, (2019/03/14)

An organometallic compound represented by Formula 1: wherein, in Formula 1, groups and variables are the same as described in the specification.

ORGANOMETALLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

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Paragraph 0454, (2019/02/02)

An organic light-emitting device includes: a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the emission layer includes an organometall

NOVEL IRIDIUM COMPLEX, ORGANIC LIGHT-EMITTING DEVICE, AND IMAGE DISPLAY APPARATUS

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Page/Page column 24; 44-46, (2011/06/26)

There is provided a novel iridium complex having a small half-width of an emission spectrum and an organic light-emitting device that contains the iridium complex. There is provided a novel iridium complex that has a phenyl ring and an imidazole ring as l

Discovery of biaryl inhibitors of H+/K+ ATPase

Garton, Neil,Bailey, Nick,Bamford, Mark,Demont, Emmanuel,Farre-Gutierrez, Irene,Hutley, Gail,Bravi, Gianpaolo,Pickering, Paula

scheme or table, p. 1049 - 1054 (2010/06/12)

We report the identification of a novel biaryl template for H+/K+ ATPase inhibition. Evaluation of critical SAR features within the biaryl imidazole framework and the use of pharmacophore modelling against known imidazopyridine and azaindole templates suggested that the geometry of the molecule is key to achieving activity. Herein we present our work optimising the potency of the molecule through modifications and substitutions to each of the ring systems. In particular sub-micromolar potency is achieved with (4b) presumably through a proposed intramolecular hydrogen bond that ensures the required imidazole basic centre is appropriately located.

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