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1,4-dihydro-2,6-dimethyl-N-phenyl-4-oxo-3-pyrancarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30546-76-0 Structure
  • Basic information

    1. Product Name: 1,4-dihydro-2,6-dimethyl-N-phenyl-4-oxo-3-pyrancarboxamide
    2. Synonyms:
    3. CAS NO:30546-76-0
    4. Molecular Formula:
    5. Molecular Weight: 243.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30546-76-0.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: 1,4-dihydro-2,6-dimethyl-N-phenyl-4-oxo-3-pyrancarboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-dihydro-2,6-dimethyl-N-phenyl-4-oxo-3-pyrancarboxamide(30546-76-0)
    11. EPA Substance Registry System: 1,4-dihydro-2,6-dimethyl-N-phenyl-4-oxo-3-pyrancarboxamide(30546-76-0)
  • 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: 30546-76-0(Hazardous Substances Data)

30546-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30546-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,4 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30546-76:
(7*3)+(6*0)+(5*5)+(4*4)+(3*6)+(2*7)+(1*6)=100
100 % 10 = 0
So 30546-76-0 is a valid CAS Registry Number.

30546-76-0Downstream Products

30546-76-0Relevant articles and documents

Process for preparing pyrone-3-carboxamide compounds

-

, (2008/06/13)

A new process for preparing a pyrone-3-carboxamide compound of the formula (IV): STR1 wherein R1 is aryl or heterocyclic group optionally substituted, R2 is alkyl, aralkyl or like group, comprising reacting a compound of the formula

REACTION OF ISOCYANIC ACID AND ISOCYANATES WITH DIKETENE. PREPARATION OF 2H-1,3-OXAZINES, 4-PYRONES, AND 2-PYRIDONES

Ozaki, Shoichiro,Nagase, Toshio,Kato, Takazo

, p. 2063 - 2066 (2007/10/02)

Reaction of diketene with isocyanic acid gave the expected product, 2,4-dioxo-6-methyl-3,4-dihydro-2H-1,3-oxazine (2), but with aryl isocyanates gave 3-aryl-2,4-dioxo-6-methyl-3,4-dihydro-2H-1,3-oxazines (3), 3-(arylcarbamoyl)-2,6-dimethyl-4-pyrones (4), and 3-acetyl-1-aryl-4-hydroxy-6-methyl-2-pyridones (5) depending on the reaction conditions.

Preparation and Antiinflammatory Activity of 2- and 4-Pyridones

Pierce, James Benjamin,Ariyan, Zaven S.,Ovenden, Gaye Stuart

, p. 131 - 136 (2007/10/02)

Several N-alkyl- and N-arylacetoamides have been self-condensed to form pyridones.N-Alkylacetoacetamides give 2-pyridones, while N-arylacetoamides give 4-pyridones.In an attempt to develop nonacidic, nonsteroidal antiinflammatory agents, the pyridones were tested in a carrageenan-induced pedal edema assay in rats.While the 2-pyridones were not active, 9 of 17 4-pyridones tested were active, and one compound (4g) had antiinflammatory efficacy in a dose-response assay (ED50 values).Most compounds were considered nontoxic by determination of approximate LD50 values in mice by a standard multidimensional observational assay.

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