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2,8-bis(ethoxycarbonyl)-5,5-difluoro-10-(2'-(3-methoxyprop-1-yn-1-yl)-5'-methyl-2-nitro-[1,1'-biphenyl]-4-yl)-1,3,7,9-tetramethyl-5H-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium-5-uide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1354546-95-4

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1354546-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1354546-95-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,4,5,4 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1354546-95:
(9*1)+(8*3)+(7*5)+(6*4)+(5*5)+(4*4)+(3*6)+(2*9)+(1*5)=174
174 % 10 = 4
So 1354546-95-4 is a valid CAS Registry Number.

1354546-95-4Relevant academic research and scientific papers

Regulating Transition-Metal Catalysis through Interference by Short RNAs

Green, Sydnee A.,Montgomery, Hayden R.,Benton, Tyler R.,Chan, Neil J.,Nelson, Hosea M.

, p. 16400 - 16404 (2019/08/26)

Herein we report the discovery of a AuI–DNA hybrid catalyst that is compatible with biological media and whose reactivity can be regulated by small complementary nucleic acid sequences. The development of this catalytic system was enabled by the discovery of a novel AuI-mediated base pair. We found that AuI binds DNA containing C-T mismatches. In the AuI–DNA catalyst's latent state, the AuI ion is sequestered by the mismatch such that it is coordinatively saturated, rendering it catalytically inactive. Upon addition of an RNA or DNA strand that is complementary to the latent catalyst's oligonucleotide backbone, catalytic activity is induced, leading to a sevenfold increase in the formation of a fluorescent product, forged through a AuI-catalyzed hydroamination reaction. Further development of this catalytic system will expand not only the chemical space available to synthetic biological systems but also allow for temporal and spatial control of transition-metal catalysis through gene transcription.

A novel fluorescent probe for Au(iii)/Au(i) ions based on an intramolecular hydroamination of a Bodipy derivative and its application to bioimaging

Wang, Jian-Bo,Wu, Qing-Qing,Min, Yuan-Zeng,Liu, Yang-Zhong,Song, Qin-Hua

, p. 744 - 746 (2012/01/19)

A novel fluorescent probe for gold ions (Au3+/Au+) is reported through blocking photoinduced electron transfer, in which a boron dipyrromethene (Bodipy) derivative reveals high selectivity and sensitivity in a gold-catalyzed intramol

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