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81118-82-3

phenyl pyruvic acid semicarbazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81118-82-3 Structure

  • Basic information

    1. Product Name: phenyl pyruvic acid semicarbazone
    2. Synonyms: phenyl pyruvic acid semicarbazone
    3. CAS NO:81118-82-3
    4. Molecular Formula:
    5. Molecular Weight: 221.216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81118-82-3.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: phenyl pyruvic acid semicarbazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl pyruvic acid semicarbazone(81118-82-3)
    11. EPA Substance Registry System: phenyl pyruvic acid semicarbazone(81118-82-3)

  • 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: 81118-82-3(Hazardous Substances Data)

81118-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81118-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,1 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81118-82:
(7*8)+(6*1)+(5*1)+(4*1)+(3*8)+(2*8)+(1*2)=113
113 % 10 = 3
So 81118-82-3 is a valid CAS Registry Number.

81118-82-3Relevant articles and documents

Synthesis and antimicrobial evaluation of 6-azauracil non-nucleosides

El-Brollosy, Nasser R.

scheme or table, p. 1483 - 1490 (2009/12/26)

The present study describes synthesis and antimicrobial evaluation of a series of novel 6-azauracil non-nucleosides. Reaction of silylated 6-azauracils with the appropriate chloroethers gave the corresponding non-nucleosides. 1-(Allyloxymethy)-6-azauracils and non-nucleosides bearing indanyl, cyclohexenyl, and cyclohexyl moieties were obtained via silylation of 6-azauracils followed by treatment with the appropriate acetals. Selected compounds were tested for their in vitro antimicrobial activity against a panel of standard strains of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Four compounds showed marked inhibitory activity particularly against the tested Gram-positive bacteria.

MOESSBAUER STUDY OF IRON(II) AND IRON(III) COMPLEXES OF SOME NITROGEN-, OXYGEN- AND SULPHUR DONOR LIGANDS. REDUCTION OF IRON(III) BY THE MERCAPTIDE GROUP

Shawney, G. L.,Baijal, J. S.,Chandra, S.,Pandeya, K. B.

, p. 325 - 332 (2007/10/02)

Complex formation reactions of iron(II) and iron(III) with semicarbazones and thiosemicarbazones of pyruvic acid and phenyl pyruvic acid have been studied by magnetic measurements and Moessbauer spectroscopy.With iron(II) all the ligands form hexa-coordin

CHROMIUM(III) COMPLEXES OF SOME NITROGEN-OXYGEN AND NITROGEN-SULPHUR DONOR LIGANDS

Chandra, Sulek,Pandeya, Krishna Bihari

, p. 419 - 424 (2007/10/02)

Chromium(III) complexes of some nitrogen-oxygen and nitrogen-sulphur donor ligands viz., phenylpyruvic acid semicarbazone (PPysc) and (4-methylphenyl)pyruvic acid semicarbazone (4-PPysc), phenylpyruvic acid thiosemicarbazone (PPytsc) and (4-methylphenyl)p

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