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6-methyl-3-[1-(phenyl-hydrazono)-ethyl]-pyran-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29214-73-1 Structure
  • Basic information

    1. Product Name: 6-methyl-3-[1-(phenyl-hydrazono)-ethyl]-pyran-2,4-dione
    2. Synonyms: 6-methyl-3-[1-(phenyl-hydrazono)-ethyl]-pyran-2,4-dione
    3. CAS NO:29214-73-1
    4. Molecular Formula:
    5. Molecular Weight: 258.277
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29214-73-1.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: 6-methyl-3-[1-(phenyl-hydrazono)-ethyl]-pyran-2,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-methyl-3-[1-(phenyl-hydrazono)-ethyl]-pyran-2,4-dione(29214-73-1)
    11. EPA Substance Registry System: 6-methyl-3-[1-(phenyl-hydrazono)-ethyl]-pyran-2,4-dione(29214-73-1)
  • 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: 29214-73-1(Hazardous Substances Data)

29214-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29214-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,1 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29214-73:
(7*2)+(6*9)+(5*2)+(4*1)+(3*4)+(2*7)+(1*3)=111
111 % 10 = 1
So 29214-73-1 is a valid CAS Registry Number.

29214-73-1Relevant articles and documents

Synthesis of some new 1-aryl-4-formyl-3-(4-hydroxy-6-methyl-2-oxo-2H-pyran- 3-yl)pyrazoles using the Vilsmeier-Haack reaction - Isolation of the key intermediate 1-aryl-3-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl) pyrazoles

Kumar, Ajay,Prakash, Om,Kinger, Mayank,Singh, Shiv P.

, p. 438 - 442 (2006)

Arylhydrazones of dehydroacetic acid (DHA) underwent Vilsmeier-Haack reaction to generate the corresponding 1-aryl-4-formyl-3-(4-hydroxy-6-methyl-2- oxo-2H-pyran-3-yl)pyrazoles (1) with the pyrone moiety of the DHA remaining intact. However, when the reac

Dehydroacetic acid hydrazinolysis

Djerrari, B.,Essassi, E.,Fifani, J.

, p. 521 - 524 (2007/10/02)

The dehydroacetic acid hydrazinolysis produces the degradation of the pyranic ring and leads to bipyrazoles.The hydrazinolysis mechanism is described.Products have been characterized by NMR, 1H, IR, MS spectra and elemental analysis.Key Words: dehydroacet

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