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58555-02-5

4H-1-Benzopyran-4-one, 6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58555-02-5 Structure

  • Basic information

    1. Product Name: 4H-1-Benzopyran-4-one, 6-phenyl-
    2. Synonyms: 4H-1-Benzopyran-4-one, 6-phenyl-;6-phenyl-4H-chromen-4-one(WXC01940)
    3. CAS NO:58555-02-5
    4. Molecular Formula: C15H10O2
    5. Molecular Weight: 222.2387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58555-02-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4H-1-Benzopyran-4-one, 6-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 6-phenyl-(58555-02-5)
    11. EPA Substance Registry System: 4H-1-Benzopyran-4-one, 6-phenyl-(58555-02-5)

  • 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: 58555-02-5(Hazardous Substances Data)

58555-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58555-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58555-02:
(7*5)+(6*8)+(5*5)+(4*5)+(3*5)+(2*0)+(1*2)=145
145 % 10 = 5
So 58555-02-5 is a valid CAS Registry Number.

58555-02-5Downstream Products

58555-02-5Relevant articles and documents

Substituent-Oriented Synthesis of Substituted Pyrazoles/Chromeno[3,2- c]pyrazoles via Sequential Reactions of Chromones/3-Chlorochromones and Tosylhydrazones

Dai, Tianzi,Li, Qunyi,Zhang, Xiaofei,Yang, Chunhao

, p. 5913 - 5921 (2019)

A facile and efficient synthetic strategy for the chemoselective synthesis of monocyclic/tricyclic-fused pyrazoles was developed, and it was oriented by different 3-position substituents (H or Cl) on the chromones. The reaction proceeded in a one-pot sequential way with a broad substrate scope and moderate to excellent yields.

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