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3,6-dibromocyclohexa-3,5-diene-1,2-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1241375-11-0

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1241375-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1241375-11-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,3,7 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1241375-11:
(9*1)+(8*2)+(7*4)+(6*1)+(5*3)+(4*7)+(3*5)+(2*1)+(1*1)=120
120 % 10 = 0
So 1241375-11-0 is a valid CAS Registry Number.

1241375-11-0Relevant academic research and scientific papers

Synthesis, characterization and properties of aryl-fused bis-BN dihydropyrenes

Zhang, Jinyun,Liu, Fude,Sun, Zhe,Li, Chenglong,Zhang, Qian,Zhang, Chen,Liu, Zhiqiang,Liu, Xuguang

, p. 8178 - 8181 (2018)

A series of aryl-fused bis-BN dihydropyrenes were synthesized via amino-directed borylation reaction. The aryl-fused bis-BN dihydropyrenes showed blue emission, and their physical properties could be finely tuned through varying the fused aryl rings. In particular, their response towards fluoride anions was greatly dependent on the nature of the fused aryl rings.

Synthesis and photovoltaic properties of two-dimensional copolymers based on novel benzothiadiazole and quinoxaline acceptors with conjugated dithienylbenzothiadiazole pendants

Huang, Yuanshuai,Ye, Linglong,Wu, Fen,Mei, Suli,Chen, Huajie,Tan, Songting

, p. 668 - 677 (2016)

Two novel acceptors of benzo[c][1,2,5]thiadiazole and quinoxaline with conjugated dithienylbenzothiadiazole pendants were first designed and synthesized for building efficient photovoltaic copolymers. Based on benzo[1,2-b;3,4-b′]dithiophene donors and the

Effects of the acceptor pattern and substitution position on the properties of N-phenyl-carbazolyl based donor-acceptor-donor molecules

Song, Xuejing,Wang, Min,Kong, Lingqian,Zhao, Jinsheng

, p. 18189 - 18198 (2017)

Four optoelectronic compounds based on the same donor (N-phenylcarbazole) and different acceptors of benzothiadiazole or benzoselenadiazole were designed and synthesized to investigate the effects of the substitution position and effects of the acceptor heteroatom on the properties of N-phenyl-carbazolyl based organic optoelectronic compounds. The results demonstrated that these four compounds have band gaps (2.25 to 2.59 eV) that are lower than that of carbazole (3.20 eV). For the acceptor moiety, the replacement of benzothiadiazole with benzoselenadiazole was beneficial for the polarization of the D-A compound. Different acceptors substituted at the 3-position of N-phenylcarbazole led to molecules with a higher degree of planar conjugation than molecules derived from acceptors substituted at the 2-position. The increase in polarity and conjugation degree of the D-A compounds gave rise to lower band gaps and redshifts in the UV-vis absorption spectra and fluorescence emission spectra compared to the corresponding compounds. Solvatochromism effects were observed for these four compounds in different polar solvents, accompanied by redshifts in the fluorescence emission spectra, which ranged from 509 nm to 596 nm. Using thermogravimetric analysis, the decomposition temperatures of all four materials were found to be above 400 °C.

Triphenylamine quinoxaline malononitrile, synthesis method thereof and method for detecting CN

-

Paragraph 0042; 0062-0063, (2021/07/01)

The invention discloses triphenylaminoquinoxaline malononitrile, a synthesis method thereof and a method for detecting CN. The molecular formula of the triphenylaminoquinoxaline malononitrile is shown in the specification. The synthesis method of the t

Side-chain engineering of green color electrochromic polymer materials: Toward adaptive camouflage application

Yu, Hongtao,Shao, Shan,Yan, Lijia,Meng, Hong,He, Yaowu,Yao, Chao,Xu, Panpan,Zhang, Xiaotao,Hu, Wenping,Huang, Wei

supporting information, p. 2269 - 2273 (2016/04/04)

The syntheses of adaptive camouflage devices based on novel side-chain engineered organic electrochromic materials have been demonstrated. Herein we report a molecule engineering approach for the tuning and syntheses of green-brown switchable electrochrom

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