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73766-16-2

4-Diethylamino-5,5-dimethyl-3-imidazolin-2-on is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73766-16-2 Structure

  • Basic information

    1. Product Name: 4-Diethylamino-5,5-dimethyl-3-imidazolin-2-on
    2. Synonyms:
    3. CAS NO:73766-16-2
    4. Molecular Formula:
    5. Molecular Weight: 183.253
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73766-16-2.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-Diethylamino-5,5-dimethyl-3-imidazolin-2-on(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Diethylamino-5,5-dimethyl-3-imidazolin-2-on(73766-16-2)
    11. EPA Substance Registry System: 4-Diethylamino-5,5-dimethyl-3-imidazolin-2-on(73766-16-2)

  • 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: 73766-16-2(Hazardous Substances Data)

73766-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73766-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,6 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73766-16:
(7*7)+(6*3)+(5*7)+(4*6)+(3*6)+(2*1)+(1*6)=152
152 % 10 = 2
So 73766-16-2 is a valid CAS Registry Number.

73766-16-2Downstream Products

73766-16-2Relevant articles and documents

Rearrangement of α-Isocyanato-N2-(arylsulfonyl)amidines to 1-Arylsulfonyl-3-imidazolin-2-ones

Schaumann, Ernst,Grabley, Susanne

, p. 934 - 940 (2007/10/02)

The reaction of the azirines 1 with the isocyanates 2 leads to the α-isocyanato-N2-(arylsulfonyl)amidines 6.Starting from 1b, also considerable amounts of 7b and 8b are formed as a result of a retro-ene reaction of 6b.The heterocumulenes 6 readily rearrange with a shift of the sulfonyl group to give the heterocycles 10.The mobility of the sulfonyl residue is also obvious from the reaction of 6a with hydrogen chloride to afford tosyl chloride and 8a as well as from the reaction with amines, which, however, does not only yield the tosylamides 15, but also the ureas13 and their secondary products 14.

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