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N-(2-(4-methoxyphenyl)-2-oxoethyl)isonicotinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

932389-85-0

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932389-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 932389-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,2,3,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 932389-85:
(8*9)+(7*3)+(6*2)+(5*3)+(4*8)+(3*9)+(2*8)+(1*5)=200
200 % 10 = 0
So 932389-85-0 is a valid CAS Registry Number.

932389-85-0Relevant academic research and scientific papers

ZINC-SELECTIVE FLUORESCENT PROBES FOR EMISSION-RATIOMETRIC IMAGING

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Paragraph 0108, (2019/01/07)

A compound according to Formula (I):, wherein Z is: (II).

VIOLET LASER EXCITABLE DYES AND THEIR METHOD OF USE

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Paragraph 0250, (2016/12/22)

The present invention provides dye compounds optimally excited at about 400 nm and have a Stokes shift of at least about 80 nm. These dyes find use in detection of analyte in a sample and the preparation of dye-conjugates.

Combinatorial discovery of novel fluorescent dyes based on Dapoxyl

Zhu, Qing,Yoon, Hai-Shin,Parikh, Puja B.,Chang, Young-Tae,Yao, Shao Q.

, p. 5083 - 5086 (2007/10/03)

We have developed a combinatorial method for the fast and effective synthesis of a library based on a known fluorescent dye, Dapoxyl using parallel solution-phase chemistry. By screening the 140 new compounds using fluorescence-based assays, we identified three new fluorescent dyes with novel properties.

Syntheses and Photophysical Properties of Some 5(2)-Aryl-2(5)-(4-pyridyl)oxazoles and Related Oxadiazoles and Furans

Hall, J. Herbert,Chien, Joseph Yuming,Kauffman, Joel M.,Litak, Peter T.,Adams, Jeffrey K.,et al.

, p. 1245 - 1273 (2007/10/02)

A number of 5-aryl-2-(4-pyridyl)oxazoles, a 2-aryl-5-(4-pyridyl)oxazole, the related oxadiazole and furan, several 2-(4-pyridyl)cycloalkanooxazoles, and many of their quaternary salts were prepared.No single standard synthesis was effective for preparation of more than a few of the 25 free bases described; methods often unique to a base were employed.Minor variations in structure sometimes produced large differences in absorption and emission wavelengths, as well as in the magnitude of the extinction coefficient.The salts are of interest as laser dyes, scintillation fluors, biological stains, and shifters for luminescent solar concentrators.

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