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1-(3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-il)etanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52217-37-5 Structure
  • Basic information

    1. Product Name: 1-(3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-il)etanone
    2. Synonyms: 1-(3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-il)etanone
    3. CAS NO:52217-37-5
    4. Molecular Formula:
    5. Molecular Weight: 265.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52217-37-5.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-(3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-il)etanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-il)etanone(52217-37-5)
    11. EPA Substance Registry System: 1-(3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-il)etanone(52217-37-5)
  • 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: 52217-37-5(Hazardous Substances Data)

52217-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52217-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,1 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52217-37:
(7*5)+(6*2)+(5*2)+(4*1)+(3*7)+(2*3)+(1*7)=95
95 % 10 = 5
So 52217-37-5 is a valid CAS Registry Number.

52217-37-5Downstream Products

52217-37-5Relevant articles and documents

Microwave-assisted one-pot synthesis in water of carbonylpyrazolo[3,4-: B] pyridine derivatives catalyzed by InCl3 and sonochemical assisted condensation with aldehydes to obtain new chalcone derivatives containing the pyrazolopyridinic moiety

Polo, Efrain,Ferrer-Pertuz, Karoll,Trilleras, Jorge,Quiroga, Jairo,Gutiérrez, Margarita

, p. 50044 - 50055 (2017)

Pyrazolo[3,4-b]pyridine derivatives have been synthesized via one-pot condensation of 3-methyl-1-phenyl-1H-pyrazolo-5-amine (1), formaldehyde (as paraformaldehyde) (2) and β-diketones (3) under microwave irradiation in aqueous media catalyzed by InCl3. This process has been found to be useful in the preparation of new N-fused heterocycle products in good to excellent yields. Further treatment of pyrazolopyridines (4a and 4e) with aldehyde aromatics (5a-l) afforded chalcone analogs.

Synthesis of newly substituted pyrazoles and substituted pyrazolo[3,4-b]pyridines based on 5-amino-3-methyl-1-phenylpyrazole

El-Emary, Talaat I.

, p. 507 - 518 (2008/02/11)

The reaction of the aminopyrazole 1 with benzenesulfonyl chloride, arenediazonium salt, chloroacetyl chloride, ethoxy methyleneamlononitrile and with ethyl 2-cyano-3-ethoxyacrylate gave the substituted 3-methyl-1- phenylpyrazole 2-5a,b. Compound 5b was cy

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