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CAS

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1268854-58-5

6-phenyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1268854-58-5 Structure

  • Basic information

    1. Product Name: 6-phenyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid
    2. Synonyms: 6-phenyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid
    3. CAS NO:1268854-58-5
    4. Molecular Formula:
    5. Molecular Weight: 234.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268854-58-5.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: 6-phenyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-phenyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid(1268854-58-5)
    11. EPA Substance Registry System: 6-phenyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid(1268854-58-5)

  • 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: 1268854-58-5(Hazardous Substances Data)

1268854-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268854-58-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,8,5 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1268854-58:
(9*1)+(8*2)+(7*6)+(6*8)+(5*8)+(4*5)+(3*4)+(2*5)+(1*8)=205
205 % 10 = 5
So 1268854-58-5 is a valid CAS Registry Number.

1268854-58-5Downstream Products

1268854-58-5Relevant articles and documents

Biginelli-type reaction: Efficient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2-ones and thiones from gem-dibromomethylarenes

Kambappa, Vinaya,Ganganahalli Kotturappa, Chandrashekara,Sheshachar Manjunath, Raghavendra,Doddakunche Shivaramu, Prasanna

, p. 3475 - 3482 (2020)

In the present study, we are reporting a simple and efficient method for the one-pot synthesis of the biologically important heterocyclic molecules 5-unsubstituted 3,4-dihydropyrimidin-2-ones and thiones using gem-dibromomethylarenes, oxalacetic acid, and urea or thiourea. Gem-dibromomethylarenes are used as aldehyde equivalent for the efficient synthesis of 3,4-dihydropyrimidin-2-ones/thiones. This reaction offers advantages for the synthesis of these compounds, including ready availability of the starting materials, experimental simplicity and in good yields. Besides, the synthesized molecules are interesting for their biological and pharmacological actions.

A rapid and convenient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2- ones and thiones

Fang, Zhanxiong,Lam, Yulin

experimental part, p. 1294 - 1297 (2011/04/12)

A rapid and convenient synthesis of 5-unsubstituted 3,4-dihydropyrimidin-2- ones and thiones was developed. The reaction involves a one-pot reaction between oxalacetic acid, thiourea/urea, and aldehyde under microwave irradiation and provides the products

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