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1311377-76-0

4-butyl-3-(4-fluorophenyl)-1-(4-methoxybenzyl)-5-propyl-1H-imidazol-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1311377-76-0 Structure

  • Basic information

    1. Product Name: 4-butyl-3-(4-fluorophenyl)-1-(4-methoxybenzyl)-5-propyl-1H-imidazol-2(3H)-one
    2. Synonyms: 4-butyl-3-(4-fluorophenyl)-1-(4-methoxybenzyl)-5-propyl-1H-imidazol-2(3H)-one
    3. CAS NO:1311377-76-0
    4. Molecular Formula:
    5. Molecular Weight: 396.505
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1311377-76-0.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-butyl-3-(4-fluorophenyl)-1-(4-methoxybenzyl)-5-propyl-1H-imidazol-2(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-butyl-3-(4-fluorophenyl)-1-(4-methoxybenzyl)-5-propyl-1H-imidazol-2(3H)-one(1311377-76-0)
    11. EPA Substance Registry System: 4-butyl-3-(4-fluorophenyl)-1-(4-methoxybenzyl)-5-propyl-1H-imidazol-2(3H)-one(1311377-76-0)

  • 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: 1311377-76-0(Hazardous Substances Data)

1311377-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1311377-76-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,3,7 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1311377-76:
(9*1)+(8*3)+(7*1)+(6*1)+(5*3)+(4*7)+(3*7)+(2*7)+(1*6)=130
130 % 10 = 0
So 1311377-76-0 is a valid CAS Registry Number.

1311377-76-0Downstream Products

1311377-76-0Relevant articles and documents

Unexpected regio- and chemoselectivity of cationic gold-catalyzed cycloisomerizations of propargylureas: Access to tetrasubstituted 3,4-dihydropyrimidin-2(1H)-ones

Pereshivko, Olga P.,Peshkov, Vsevolod A.,Peshkov, Anatoly A.,Jacobs, Jeroen,Van Meervelt, Luc,Van Der Eycken, Erik V.

, p. 1741 - 1750 (2014/03/21)

Cationic gold-catalyzed cycloisomerizations of propargylureas, derived in situ from secondary propargylamines and aryl or alkyl isocyanates, have been studied. The reaction outcome was found to be different from what was previously observed for the tosyl isocyanate-derived ureas in terms of both regio- and chemoselectivity. As a result, the current protocol offers efficient access to the 3,4-dihydropyrimidin-2(1H)-one core through the 6-endo-dig N-cyclization.

Tetrasubstituted 2-imidazolones via ag(I)-catalyzed cycloisomerization of propargylic ureas

Peshkov, Vsevolod A.,Pereshivko, Olga P.,Sharma, Sweta,Meganathan, Thirumal,Parmar, Virinder S.,Ermolat'Ev, Denis S.,Van Der Eycken, Erik V.

, p. 5867 - 5872 (2011/09/14)

A one-pot protocol based on a Ag(I)-catalyzed cycloisomerization of propargylic ureas, derived from secondary propargylamines and isocyanates, was developed for the generation of the 2-imidazolone core.

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