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1084890-31-2

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1084890-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1084890-31-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,4,8,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1084890-31:
(9*1)+(8*0)+(7*8)+(6*4)+(5*8)+(4*9)+(3*0)+(2*3)+(1*1)=172
172 % 10 = 2
So 1084890-31-2 is a valid CAS Registry Number.

1084890-31-2Relevant academic research and scientific papers

FLUORESCENT PROBE FOR ALDH3A1 DETECTION

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Paragraph 0131, (2020/07/16)

[Problem to be Solved] To provide a fluorescent probe for ALDH3A1 detection that can be used in flow cytometry adaptable to live cells. [Means of Resolution] A compound represented by general formula (I) or a salt thereof, wherein the compound or salt the

Chemical synthesis of mono- and bis-labeled pre-MicroRNAs

Pradere, Ugo,Brunschweiger, Andreas,Gebert, Luca F. R.,Lucic, Matije,Roos, Martina,Hall, Jonathan

supporting information, p. 12028 - 12032 (2013/12/04)

A chemical method for the post-synthetic labeling of pre-miRNAs on solid support using easily accessible reagents was developed. The procedure was employed to generate a library of 31 pre-microRNAs carrying labels commonly used in chemical biology, including Cy3, trioxalen, biotin, and BHQ-1. Copyright

Water-soluble, deep-red fluorescent squaraine rotaxanes

Cole, Erin L.,Arunkumar, Easwaran,Xiao, Shuzhang,Smith, Bryan A.,Smith, Bradley D.

supporting information; experimental part, p. 5769 - 5773 (2012/08/28)

Eight fluorescent squaraine rotaxanes with deep-red absorption/emission wavelengths were prepared and assessed for chemical stability and suitability as water-soluble, fluorescent tracers. The most stable squaraine rotaxanes have four large stopper groups attached to the ends of the encapsulated squaraine, and two members of this structural class have promise as highly fluorescent tracers with rapid renal clearance and very low tissue uptake in living mice.

Near-infrared solid-state emitters based on isophorone: Synthesis, crystal structure and spectroscopic properties

Massin, Julien,Dayoub, Wissam,Mulatier, Jean-Christophe,Aronica, Christophe,Bretonniere, Yann,Andraud, Chantal

experimental part, p. 862 - 873 (2012/02/14)

A series of near-infrared solid-state emitters based on the dicyanoisophorone electron acceptor group was synthesized. The solid-state spectroscopic properties were studied by UV-visible absorption spectroscopy and fluorescence spectroscopy and analyzed i

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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