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1-(3-hydroxyphenyl)isoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134948-98-4

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134948-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134948-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134948-98:
(8*1)+(7*3)+(6*4)+(5*9)+(4*4)+(3*8)+(2*9)+(1*8)=164
164 % 10 = 4
So 134948-98-4 is a valid CAS Registry Number.

134948-98-4Relevant academic research and scientific papers

Bifunctional organocatalysts for the enantioselective synthesis of axially chiral isoquinoline n -oxides

Miyaji, Ryota,Asano, Keisuke,Matsubara, Seijiro

, p. 6766 - 6769 (2015)

Bifunctional catalysts bearing amino and urea functional groups have been applied for a novel, highly enantioselective synthesis of axially chiral isoquinoline N-oxides, which are promising chiral ligands or organocatalysts in organic synthesis. This is t

TETRADENTATE AND OCTAHEDRAL METAL COMPLEXES CONTAINING NAPHTHYRIDINOCARBAZOLE AND ITS ANALOGUES

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, (2016/12/26)

Tetradentate and octahedral metal complexes suitable for use as phosphorescent or delayed fluorescent and phosphorescent emitters in display and lighting applications.

NOVEL TETRADENTATE PLATINUM COMPLEXES

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, (2012/09/11)

Novel phosphorescent tetradentate platinum (II) compounds comprising a twisted aryl group are provided. Also provided are novel phosphorescent tetradentate platinum (II) compounds comprising an imidazo[1,2-f]phenanthridine moiety. The compounds may be used in organic light emitting devices to provide improved device efficiency, line shape and lifetime.

1H and 13C NMR Spectra of Fifteen Substituted Isoquinolines

Nelson, Janis T.,Davis, Roman

, p. 513 - 517 (2007/10/02)

Detailed analyses of the 1H and 13C NMR spectra of fifteen momo- and di-substituted isoquinoline derivatives were carried out by two-dimensional 1H-1H and 1H-13C shift correlation and nuclear Overhauser effect difference techniques.

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