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1411975-51-3

C8H5N3O6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1411975-51-3 Structure

  • Basic information

    1. Product Name: C8H5N3O6
    2. Synonyms:
    3. CAS NO:1411975-51-3
    4. Molecular Formula:
    5. Molecular Weight: 239.144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1411975-51-3.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: C8H5N3O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C8H5N3O6(1411975-51-3)
    11. EPA Substance Registry System: C8H5N3O6(1411975-51-3)

  • 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: 1411975-51-3(Hazardous Substances Data)

1411975-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1411975-51-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,1,9,7 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1411975-51:
(9*1)+(8*4)+(7*1)+(6*1)+(5*9)+(4*7)+(3*5)+(2*5)+(1*1)=153
153 % 10 = 3
So 1411975-51-3 is a valid CAS Registry Number.

1411975-51-3Downstream Products

1411975-51-3Relevant articles and documents

Direct Henry reactions with modified calcium oxide as solid catalyst

Tang, Ying,Gu, Xuefan,Meng, Mei,Xu, Jingfang

, p. 3715 - 3725 (2013)

Commercial CaO was modified simply with benzyl bromide. The modified CaO had good water resistance, and characterization by FTIR and TG revealed the modifier was chemically bonded to the CaO surface. Commercial CaO and CaO modified with benzyl bromide were investigated as catalysts for the Henry reaction between benzaldehyde and nitromethane. It was found that the catalytic activity of the modified CaO was greatly improved, with high conversion of benzaldehyde to the (E)-phenyl nitroolefin and 1-phenyl-2-nitroethanol, and with different selectivity from commercial CaO. The effect of modification and reaction conditions on yield, selectivity, and mechanism were studied thoroughly.

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