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1146216-13-8

4-(morpholin-4-yl)-5-nitro-1-phenacylimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1146216-13-8 Structure

  • Basic information

    1. Product Name: 4-(morpholin-4-yl)-5-nitro-1-phenacylimidazole
    2. Synonyms:
    3. CAS NO:1146216-13-8
    4. Molecular Formula:
    5. Molecular Weight: 316.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1146216-13-8.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: 4-(morpholin-4-yl)-5-nitro-1-phenacylimidazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(morpholin-4-yl)-5-nitro-1-phenacylimidazole(1146216-13-8)
    11. EPA Substance Registry System: 4-(morpholin-4-yl)-5-nitro-1-phenacylimidazole(1146216-13-8)

  • 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: 1146216-13-8(Hazardous Substances Data)

1146216-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146216-13-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,2,1 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1146216-13:
(9*1)+(8*1)+(7*4)+(6*6)+(5*2)+(4*1)+(3*6)+(2*1)+(1*3)=118
118 % 10 = 8
So 1146216-13-8 is a valid CAS Registry Number.

1146216-13-8Downstream Products

1146216-13-8Relevant articles and documents

Synthesis of some N-substituted nitroimidazole derivatives as potential antioxidant and antifungal agents

Olender, Dorota,Zwawiak, Justyna,Lukianchuk, Victor,Lesyk, Roman,Kropacz, Aleksandra,Fojutowski, Andrzej,Zaprutko, Lucjusz

experimental part, p. 645 - 652 (2009/09/08)

Some new nitroimidazole derivatives have been synthesized by treating 4,5-dinitro- and 2-methyl-4,5-dinitroimidazoles with epoxypropane, epichlorohydrin or phenacyl bromide in alkylation reactions. The nitro group in N-substituted 4,5-dinitro- and 2-methyl-4,5-dinitroimidazoles has been replaced with primary and secondary amines to afford 4-amino-5-nitroimidazole derivatives. Some of the compounds have been tested for their antioxidant and antifungal properties against fungi species acting on timber. Nearly all of them have shown significant antioxidant activity in comparison with that of tocopherol, which is used as a reference substance. Two compounds from those tested have revealed very strong fungistatic activity against Sclerophoma pityophila.

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