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N-ethyl-N-(2-azidoethyl)-4-(4-nitrophenylazo)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

342395-45-3

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342395-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342395-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,3,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 342395-45:
(8*3)+(7*4)+(6*2)+(5*3)+(4*9)+(3*5)+(2*4)+(1*5)=143
143 % 10 = 3
So 342395-45-3 is a valid CAS Registry Number.

342395-45-3Downstream Products

342395-45-3Relevant academic research and scientific papers

New "X-type" second-order nonlinear optical (NLO) dendrimers: Fewer chromophore moieties and high NLO effects

Tang, Runli,Zhou, Shengmin,Xiang, Wendi,Xie, Yujun,Chen, Hong,Peng, Qian,Yu, Gui,Liu, Binwen,Zeng, Huiyi,Li, Qianqian,Li, Zhen

, p. 4545 - 4552 (2015)

New types of "X-type" NLO dendrimers, C2 and C3, in which the chromophore moieties were arranged in order, were rationally designed. The special topology of the chromophore moieties contributed a great deal to the good NLO performance of C2 and C3: the d33 value of C2 (containing only five chromophore moieties) was 157.4 pm V-1, while that of C3 (containing nine chromophore moieties) achieved 195.2 pm V-1, much larger than that of C1 (74.7 pm V-1, containing three chromophore moieties) and the fifth generation dendrimer (G5) (193.1 pm V-1, bearing 62 pieces of chromophore moieties). Through careful experimental and theoretical analysis, their structure-property relationship was explained, and discussed in detail.

NOVEL CHROMOPHORIC SILYL PROTECTING GROUPS AND THEIR USE IN THE CHEMICAL SYNTHESIS OF OLIGONUCLEOTIDES

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Page/Page column 19-20; sheet 5, (2009/01/20)

The present invention provides compounds of the formula (I): C-Q-O-Si (R1)(R2)-N wherein C is a chromophore; Q is selected from the group consisting of optionally substituted aliphatic, aryl, heteroaryl, cycloalkyl or heterocycloalkyl; R1 and R2 are independently selected from the group consisting of optionally substituted C1-8 alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, C1-8 alkyloxy, cycloalkyloxy, heterocycloalkyloxy, alkylsilyloxy and arylsilyloxy; and N is a glycosylamine or abasic moiety.

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