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332102-75-7

2-(4-tert-butylphenyl)-6-methyl-4H-chromen-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 332102-75-7 Structure

  • Basic information

    1. Product Name: 2-(4-tert-butylphenyl)-6-methyl-4H-chromen-4-one
    2. Synonyms: 2-(4-tert-butylphenyl)-6-methyl-4H-chromen-4-one
    3. CAS NO:332102-75-7
    4. Molecular Formula: C20H20O2
    5. Molecular Weight: 292.3716
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 332102-75-7.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: 2-(4-tert-butylphenyl)-6-methyl-4H-chromen-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-tert-butylphenyl)-6-methyl-4H-chromen-4-one(332102-75-7)
    11. EPA Substance Registry System: 2-(4-tert-butylphenyl)-6-methyl-4H-chromen-4-one(332102-75-7)

  • 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: 332102-75-7(Hazardous Substances Data)

332102-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332102-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,1,0 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 332102-75:
(8*3)+(7*3)+(6*2)+(5*1)+(4*0)+(3*2)+(2*7)+(1*5)=87
87 % 10 = 7
So 332102-75-7 is a valid CAS Registry Number.

332102-75-7Downstream Products

332102-75-7Relevant articles and documents

Construction of the flavones and aurones through regioselective carbonylative annulation of 2-bromophenols and terminal alkynes

Liu, Jianming,Liu, Muwen,Yue, Yuanyuan,Zhang, Ningfei,Zhang, Yuanli,Zhuo, Kelei

supporting information, p. 1802 - 1807 (2013/04/24)

The easily available and efficient catalyst containing a benzimidazolium ligand and PdCl2(PPh3)2 demonstrated excellent catalytic activity to construct the flavones and aurones, respectively. This reaction can be operated under mild conditions, affording the desired products in moderate to good yields. This protocol was used to prepare the flavones and aurones by a slight modification of amines.

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