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2-(p-methoxyphenyl)ethan-1,2-dion-1-oxime sodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151427-04-2 Structure
  • Basic information

    1. Product Name: 2-(p-methoxyphenyl)ethan-1,2-dion-1-oxime sodium salt
    2. Synonyms: 2-(p-methoxyphenyl)ethan-1,2-dion-1-oxime sodium salt
    3. CAS NO:151427-04-2
    4. Molecular Formula:
    5. Molecular Weight: 201.157
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151427-04-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(p-methoxyphenyl)ethan-1,2-dion-1-oxime sodium salt(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(p-methoxyphenyl)ethan-1,2-dion-1-oxime sodium salt(151427-04-2)
    11. EPA Substance Registry System: 2-(p-methoxyphenyl)ethan-1,2-dion-1-oxime sodium salt(151427-04-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 151427-04-2(Hazardous Substances Data)

151427-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151427-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,4,2 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 151427-04:
(8*1)+(7*5)+(6*1)+(5*4)+(4*2)+(3*7)+(2*0)+(1*4)=102
102 % 10 = 2
So 151427-04-2 is a valid CAS Registry Number.

151427-04-2Upstream product

151427-04-2Relevant articles and documents

Facile synthesis of 6-aryl-3-pyridyl-1,2,4-triazines as a key step toward highly fluorescent 5-substituted bipyridines and their Zn(II) and Ru(II) complexes

Kozhevnikov, Valery N.,Shabunina, Olga V.,Kopchuk, Dmitry S.,Ustinova, Maria M.,K?nig, Burkhard,Kozhevnikov, Dmitry N.

, p. 8963 - 8973 (2008/12/22)

A wide series of substituted bipyridines were obtained through the synthesis of 1,2,4-triazines and their aza Diels-Alder reactions. The reported method facilitates the synthesis of functionally diverse bipyridines that provides fine-tuning of photophysical properties of new ligands and their Zn(II) and Ru(II) complexes. Some of substituted bipyridines exhibit 'off-on' fluorescence response toward Zn2+ cations.

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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