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9-phenyl-9H-carbazol-3-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1318253-36-9

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1318253-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1318253-36-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,8,2,5 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1318253-36:
(9*1)+(8*3)+(7*1)+(6*8)+(5*2)+(4*5)+(3*3)+(2*3)+(1*6)=139
139 % 10 = 9
So 1318253-36-9 is a valid CAS Registry Number.

1318253-36-9Downstream Products

1318253-36-9Relevant academic research and scientific papers

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

-

, (2019/07/18)

The present invention provides a compound of chemical formula 1 and an organic light emitting device comprising the same. The compound according to the present invention has excellent electrochemical and thermal stability, thereby having excellent lifespan characteristics.COPYRIGHT KIPO 2019

Carbazole derivative, preparation method, and application thereof

-

, (2017/06/02)

The invention provides a carbazole derivative, a preparation method, and an application thereof, and relates to the technical field of organic photoelectric materials. Through introduction of a condensed-ring rigid and dense structure, the carbazole deriv

Carbazole N-substituent effect upon DTMA: Stabilizing and photochromic modulating

Huo, Zhiming,Li, Zhipeng,Wang, Tingting,Zeng, Heping

, p. 8964 - 8973 (2013/09/23)

Dithienylmaleimide derivatives 7-27 were synthesized by introducing N-substituted carbazole for photo-stabilizing purpose, and the structures were fully confirmed. The photochromism and photo-stability were recorded via UV-vis spectra. Only ortho compounds 8-17 with N-substituents on carbazole moiety showed escalated photochromic change, while compound 7 and the para counterparts 18-27 showed no appreciable photochromism. Additionally, compounds 8-18 exhibited good photo-stability except 17 under 254 nm irradiation. The unstability of 17 may probably due to overrunning hindrance. These photochromic patterns indicated that hindrance and electronic effect mutually paid a decisive influence on the photochromism and photo-stability, which potentially exploited a new way to construct novel photochromic materials with regulable and conceivable performance.

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