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ethyl 4,7-diphenyl-1,2,5-oxadiazolo<3,4-c>pyridine-6-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76593-55-0

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76593-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76593-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,9 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76593-55:
(7*7)+(6*6)+(5*5)+(4*9)+(3*3)+(2*5)+(1*5)=170
170 % 10 = 0
So 76593-55-0 is a valid CAS Registry Number.

76593-55-0Relevant academic research and scientific papers

ALKOXYSILYL GROUP-CONTAINING ORGANIC EL DYE AND A METHOD FOR PRODUCING THE SAME

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Paragraph 0072; 0075, (2017/11/16)

Provided is an alkoxysilyl group-containing organic EL dye that can be used for the production of fluorescent silica particles that do not fade. This alkoxysilyl group-containing organic EL dye is represented by the general formula X—Y-Q-Z—Si(R1/sub

10-Hydroxy-7-arylindeno[1,2-b]-1,2,5-oxadiazolo[3,4-d]pyridines and 7- aryl-10-oxoindeno[1,2-b]-1,2,5-oxadiazolo[3,4-d]pyridines-synthesis, spectra, and polymorphism

Mataka, Shuntaro,Gorohmaru, Hideki,Thiemann, Thies,Sawada, Tsuyoshi,Takahashi, Kazufumi,Tori-i, Akiyoshi

, p. 895 - 902 (2007/10/03)

The novel dyes 7-aryl- 10-oxoindeno[1,2-b]-1,2,5-oxadiazolo[3,4-d]- pyridines (4) and 7-aryl-10-hydroxyindeno[1,2-b]-1,2,5-oxadiazolo[3,4-d]- pyridines (5) have been prepared from acetophenone derivatives. While compounds (4) exhibit a dark red color, the

Reduction of 4,7-Diphenyl-1,2,5-thia(oxa)diazolopyridines Affording 2,5-Diphenyl-3,4-diaminopyridines and Ring Closure of the Diamines to Fluorescent Azaheterocycles

Mataka, Shuntaro,Takahashi, Kazufumi,Imura, Tetsuro,Tashiro, Masashi

, p. 1481 - 1488 (2007/10/02)

Reduction of 4,7-diphenyl-1,2,5-thia- (1a-i) and 1,2,5-oxadiazolopyridines (3a and c-e) gave 3,4-diamino-2,5-diphenylpyridines (2a-g), which were converted into the fluorescent triazolo- (5), 1,2,5-selenadiazolo- (6), imidazolo

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