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354119-58-7

3-allyl-5-benzylidene-1-methyl-2-thioxo-4-imidazolidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 354119-58-7 Structure

  • Basic information

    1. Product Name: 3-allyl-5-benzylidene-1-methyl-2-thioxo-4-imidazolidinone
    2. Synonyms: 3-allyl-5-benzylidene-1-methyl-2-thioxo-4-imidazolidinone
    3. CAS NO:354119-58-7
    4. Molecular Formula: C14H14N2OS
    5. Molecular Weight: 258.33876
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 354119-58-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-allyl-5-benzylidene-1-methyl-2-thioxo-4-imidazolidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-allyl-5-benzylidene-1-methyl-2-thioxo-4-imidazolidinone(354119-58-7)
    11. EPA Substance Registry System: 3-allyl-5-benzylidene-1-methyl-2-thioxo-4-imidazolidinone(354119-58-7)

  • 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: 354119-58-7(Hazardous Substances Data)

354119-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 354119-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,1,1 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 354119-58:
(8*3)+(7*5)+(6*4)+(5*1)+(4*1)+(3*9)+(2*5)+(1*8)=137
137 % 10 = 7
So 354119-58-7 is a valid CAS Registry Number.

354119-58-7Downstream Products

354119-58-7Relevant articles and documents

Synthesis of thiohydantoins by phosphine-catalyzed reaction of thioureas with arylpropiolates

Carboni, Michael,Gomis, Jean-Marie,Loreau, Olivier,Taran, Frederic

, p. 417 - 424 (2008/09/20)

A simple and efficient method for constructing thiohydantoin heterocycles using a phosphine-catalyzed tandem umpolung addition and intramolecular cyclization of thioureas on arylpropiolates is described. Georg Thieme Verlag Stuttgart.

Synthesis of 3-substituted 5-arylidene-1-methyl-2-Thiohydantoins under microwave irradiation

Khodair, Ahmed I.,Nielsen, John

, p. 1017 - 1032 (2007/10/03)

A mono-modal microwave oven was used to expedite the synthesis of small libraries of 3-substituted 1-methyl-2-thiohydantoins and 3-substituted 5-arylidene-1-methyl-2-thiohydantoins. In comparison with the traditional reflux methods, similar or higher yields were obtained.

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