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1383550-08-0

(Z)-5-benzyl-5-(2-ethylbut-2-enyl)-2-thioxo-dihydropyrimidine-4,6(1H,5H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1383550-08-0 Structure

  • Basic information

    1. Product Name: (Z)-5-benzyl-5-(2-ethylbut-2-enyl)-2-thioxo-dihydropyrimidine-4,6(1H,5H)-dione
    2. Synonyms:
    3. CAS NO:1383550-08-0
    4. Molecular Formula:
    5. Molecular Weight: 316.424
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1383550-08-0.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: (Z)-5-benzyl-5-(2-ethylbut-2-enyl)-2-thioxo-dihydropyrimidine-4,6(1H,5H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-5-benzyl-5-(2-ethylbut-2-enyl)-2-thioxo-dihydropyrimidine-4,6(1H,5H)-dione(1383550-08-0)
    11. EPA Substance Registry System: (Z)-5-benzyl-5-(2-ethylbut-2-enyl)-2-thioxo-dihydropyrimidine-4,6(1H,5H)-dione(1383550-08-0)

  • 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: 1383550-08-0(Hazardous Substances Data)

1383550-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383550-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,5,5 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1383550-08:
(9*1)+(8*3)+(7*8)+(6*3)+(5*5)+(4*5)+(3*0)+(2*0)+(1*8)=160
160 % 10 = 0
So 1383550-08-0 is a valid CAS Registry Number.

1383550-08-0Upstream product

1383550-08-0Downstream Products

1383550-08-0Relevant articles and documents

New methodology for the synthesis of thiobarbiturates mediated by manganese(III) acetate

Bouhlel, Ahlem,Curti, Christophe,Vanelle, Patrice

, p. 4313 - 4325 (2012)

A three step synthesis of various thiobarbiturate derivatives 17-24 was established. The first step is mediated by Mn(OAc)3, in order to generate a carbon-carbon bond between a terminal alkene and malonate. Derivatives 1-8 were obtained in moderate to good yields under mild conditions. This key step allows synthesis of a wide variety of lipophilic thiobarbiturates, which could be tested for their anticonvulsive or anesthesic potential.

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