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80820-84-4

1-tert-Butyl-3-phenyl-5-(4-tolyl)biuret is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80820-84-4 Structure

  • Basic information

    1. Product Name: 1-tert-Butyl-3-phenyl-5-(4-tolyl)biuret
    2. Synonyms:
    3. CAS NO:80820-84-4
    4. Molecular Formula:
    5. Molecular Weight: 325.411
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80820-84-4.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-tert-Butyl-3-phenyl-5-(4-tolyl)biuret(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-tert-Butyl-3-phenyl-5-(4-tolyl)biuret(80820-84-4)
    11. EPA Substance Registry System: 1-tert-Butyl-3-phenyl-5-(4-tolyl)biuret(80820-84-4)

  • 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: 80820-84-4(Hazardous Substances Data)

80820-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80820-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80820-84:
(7*8)+(6*0)+(5*8)+(4*2)+(3*0)+(2*8)+(1*4)=124
124 % 10 = 4
So 80820-84-4 is a valid CAS Registry Number.

80820-84-4Downstream Products

80820-84-4Relevant articles and documents

Reactions of N1-Hydroxyformamidines with Heterocumulenes

Zinner, Gerwalt,Schecker, Heinz-Guenther,Heuer, Wilhelm

, p. 1006 - 1014 (2007/10/02)

N1-Hydroxyformamidines and isocyanates react to yield N1-(carbamoyloxy)formamidines and/or 3-amino-1,2,4-oxazolidin-5-ones.Frequently the formation of ureas is observed.It can be explained by an oxidoreductive rearrangement to 1,3,5-trisubstituted biurets which undergo abstraction of isocyanate.Reactions with carbodiimides lead to 3-amino-5-imino-1,2,4-oxadiazolidines, ureas and carbodiimides not identical with the educts.

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