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3-bromo-2-methyl-5-(4-(trifluoromethyl)phenyl)thiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1374693-91-0

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1374693-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374693-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,6,9 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1374693-91:
(9*1)+(8*3)+(7*7)+(6*4)+(5*6)+(4*9)+(3*3)+(2*9)+(1*1)=200
200 % 10 = 0
So 1374693-91-0 is a valid CAS Registry Number.

1374693-91-0Relevant academic research and scientific papers

Photochromism of new unsymmetrical diarylethenes with a quinoline moiety

Liu, Peng,Liu, Hongliang,Liu, Gang,Zhang, Zhihui,Xu, Fen,Pu, Shouzhi

, (2017)

Three unsymmetrical diarylethenes with a 6-membered quinoline moiety were synthesized to investigate the effects of the substituents on their photochromism, and fluorescence, and the structure of one diarylethene was determined by single crystal X-ray dif

Sensitive Assays by Nucleophile-Induced Rearrangement of Photoactivated Diarylethenes

Fredrich, Sebastian,Bonasera, Aurelio,Valderrey, Virginia,Hecht, Stefan

supporting information, p. 6432 - 6440 (2018/05/31)

Upon light-induced isomerization, diarylethenes (DAEs) equipped with reactive aldehyde moieties rearrange selectively in the presence of amines, accompanied by decoloration. In a comprehensive study, the probe structure was optimized with regard to its inherent reactivity in the nucleophile-triggered rearrangement reaction. Detailed structure-reactivity relationships could be derived, in particular with regard to the type of integrated (het)aryl moieties as well as the location of the formyl residue, and the probes' intrinsic reactivity with primary and secondary amines was optimized. Utilizing an ancillary base, the initially formed rearrangement product can engage in a subsequent catalytic cycle, leading to an amplified decoloration process. This additional catalytic pathway allows us to enhance the sensitivity of our method and successfully discriminate between amines and thiols. Moreover, probes that exhibit strong analyte-induced fluorescence modulation have been designed to further decrease the detection limit by using a more sensitive read-out. The optimized DAE probes are promising molecular components for future programmable sensing materials and devices.

Photochromism of new unsymmetrical diarylethenes with an indazole moiety

Liu, Jingjing,Liu, Hongliang,Pu, Shouzhi

supporting information, p. 5223 - 5227 (2015/08/19)

A new class of photochromic diarylethenes with an indazole moiety has been firstly synthesized, and their photochromic and fluorescence properties have been investigated. The indazole moiety was connected directly to the central cyclopentene ring as one h

Photochromism of asymmetrical diarylethenes with a pyrimidine unit: Synthesis and substituent effects

Liu, Hongliang,Pu, Shouzhi,Liu, Gang,Chen, Bing

, p. 159 - 168 (2014/01/06)

Abstract Five photochromic diarylethenes with a six-membered pyrimidine moiety were synthesized to investigate the effects of the substituents on their photochromic behaviors, and the structures of four of the diarylethenes were determined by single-cryst

New photochromic diarylethenes with a pyrimidine moiety

Liu, Hongliang,Pu, Shouzhi,Liu, Gang,Chen, Bing

supporting information, p. 646 - 650 (2013/02/23)

A novel class of photochromic diarylethene derivatives based on the hybrid skeleton of six-membered pyrimidine and five-membered thiophene moieties has been firstly synthesized. The substituent effects on their properties, including photochromism, fatigue

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