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126474-02-0

8-Phenyl-5,8-dihydro-6H-pyrano[3,4-b]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126474-02-0 Structure

  • Basic information

    1. Product Name: 8-Phenyl-5,8-dihydro-6H-pyrano[3,4-b]pyridine
    2. Synonyms:
    3. CAS NO:126474-02-0
    4. Molecular Formula:
    5. Molecular Weight: 211.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126474-02-0.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: 8-Phenyl-5,8-dihydro-6H-pyrano[3,4-b]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-Phenyl-5,8-dihydro-6H-pyrano[3,4-b]pyridine(126474-02-0)
    11. EPA Substance Registry System: 8-Phenyl-5,8-dihydro-6H-pyrano[3,4-b]pyridine(126474-02-0)

  • 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: 126474-02-0(Hazardous Substances Data)

126474-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126474-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,7 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126474-02:
(8*1)+(7*2)+(6*6)+(5*4)+(4*7)+(3*4)+(2*0)+(1*2)=120
120 % 10 = 0
So 126474-02-0 is a valid CAS Registry Number.

126474-02-0Downstream Products

126474-02-0Relevant articles and documents

INTRAMOLECULAR INVERSE ELECTRON DEMAND DIELS-ALDER REACTIONS OF PYRAZINES

Biedrzycki, Marek,Bie, Dick A. de,Plas, Henk C. van der

, p. 6211 - 6220 (2007/10/02)

Thermally induced intramolecular Diels-Alder cyclisations of (alkynyloxyalkyl)pyrazines to dihydropyranopyridines have been studied in the solvent undecane.The introduction of a phenyl group in the α-position of the 3-butynyloxymethyl side chain leads to a 3-4 fold increase of the reaction rate, while the influence of a γ-phenyl group on the rate is negligible.The (3-butynyloxymethyl)pyrazine reacts about 7 times slower than the (3-propynyloxyethyl)pyrazine; the presence of a trimethylsilyl group at the terminus of the alkyne decreases in general the rate of the intramolecular cyclisation.The mechanisms are discussed.

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