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154422-03-4

1-(4-Hydroxy-7-methyl-5-oxo-5H-furo[3,2-g]chromen-9-yl)-3-phenyl-thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154422-03-4 Structure

  • Basic information

    1. Product Name: 1-(4-Hydroxy-7-methyl-5-oxo-5H-furo[3,2-g]chromen-9-yl)-3-phenyl-thiourea
    2. Synonyms:
    3. CAS NO:154422-03-4
    4. Molecular Formula:
    5. Molecular Weight: 366.397
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154422-03-4.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-(4-Hydroxy-7-methyl-5-oxo-5H-furo[3,2-g]chromen-9-yl)-3-phenyl-thiourea(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Hydroxy-7-methyl-5-oxo-5H-furo[3,2-g]chromen-9-yl)-3-phenyl-thiourea(154422-03-4)
    11. EPA Substance Registry System: 1-(4-Hydroxy-7-methyl-5-oxo-5H-furo[3,2-g]chromen-9-yl)-3-phenyl-thiourea(154422-03-4)

  • 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: 154422-03-4(Hazardous Substances Data)

154422-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154422-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,4,2 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 154422-03:
(8*1)+(7*5)+(6*4)+(5*4)+(4*2)+(3*2)+(2*0)+(1*3)=104
104 % 10 = 4
So 154422-03-4 is a valid CAS Registry Number.

154422-03-4Downstream Products

154422-03-4Relevant articles and documents

Synthesis, anticonvulsant and antimicrobial activities of certain new furochromones

Ragab,Hussein,Hanna,Hassan,Kenawy

, p. 808 - 811 (2007/10/02)

Some new substituted thiazolidinones, thioimidazolidinones and thiazolines have been synthesized from N1-substituted N2-(4-hydroxy-7-methyl-5H-furo[3,2-g] [1]benzopyran-5-on-9-yl)thioureas and monochloroacetic acid or α-halocarbonyl

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