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23281-41-6

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23281-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23281-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,8 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23281-41:
(7*2)+(6*3)+(5*2)+(4*8)+(3*1)+(2*4)+(1*1)=86
86 % 10 = 6
So 23281-41-6 is a valid CAS Registry Number.

23281-41-6Relevant academic research and scientific papers

Synthesis and Characterization of Squaraine-Based Photocrosslinkable Resists for Bulk Heterojunction Solar Cells

Turrisi, Riccardo,Mascheroni, Luca,Sassi, Mauro,Rooney, Myles,Buccheri, Nunzio,Ruffo, Riccardo,Facchetti, Antonio,Beverina, Luca

, p. 4032 - 4040 (2016/08/24)

Organic photovoltaic devices (OPVs) are rapidly approaching the commercialization threshold thanks to continuous advances in conversion efficiencies and device durability. Even though the design of high performing active dyes (polymeric and molecular) has

Novel Nile Blue derivatives as fluorescent probes for DNA

Rama Raju,Naik, Sarala,Coutinho, Paulo J.G.,Gon?alves, M. Sameiro T.

, p. 220 - 227 (2013/10/21)

Cationic dyes based on benzo[a]phenoxazinium chlorides either mono- or disubstituted with ethyl, octyl and dodecyl groups at the amino side chain at the 9-position of the tetracyclic ring, and possessing a propyl group at the 5-amino position were synthesised, characterised and used in photophysical studies with DNA and in agarose gel electrophoresis assays. Photophysical results showed that compounds with diethyl and octyl substituents intercalated in DNA above a phosphate dye ratio of 10. All compounds associated with DNA as evidenced by their use as coloured markers of migrating DNA bands in agarose gel electrophoresis experiments.

[(CyPF-Bu)PdCI2]: An air-stable, one-component, highly efficient catalyst for amination of heteroaryl and aryl halides

Shen, Qilong,Hartwig, John F.

supporting information; experimental part, p. 4109 - 4112 (2009/05/27)

(Chemical Equation Presented) An air- and moisture-stable palladium catalyst, [(CyPF-1Bu)PdCI2] (1), for coupling of heteroaryl chlorides, bromides, and iodides with a variety of primary amines is described. Most of these reactions occurred in high yield with 0.001-0.05 mol % catalyst loading. The reactions tolerated a wide range of functional groups.

Highly reactive, general, and long-lived catalysts for coupling heteroaryl and aryl chlorides with primary nitrogen nucleophiles

Shen, Qilong,Shekhar, Shashank,Stambuli, James P.,Hartwig, John F.

, p. 1371 - 1375 (2007/10/03)

Resisting pathways for decomposition followed by palladium complexes of monodentate ligands is one characteristic of the highly reactive but long-lived catalyst generated from the Josiphos ligand L and palladium. It catalyzes under mild conditions the coupling of primary amines with chloropyridines and chloroarenes in high yield with low catalyst loadings (see scheme).

The autorecycling oxidation of benzylamine by synthetic 8-hydroxy-5-deazaflavin derivatives

Hirayama,Kawase,Kimachi,Tanaka,Yoneda

, p. 1255 - 1259 (2007/10/02)

Various 8-hydroxy-5-deazaflavin derivatives were synthesized as the model compounds of coenzyme F420. These compounds oxidized benzylamine to benzaldehyde more efficiently than the corresponding 8-unsubstituted 5-deazaflavin.

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