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134141-09-6

ethyl 4-(2-chlorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134141-09-6 Structure

  • Basic information

    1. Product Name: ethyl 4-(2-chlorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
    2. Synonyms:
    3. CAS NO:134141-09-6
    4. Molecular Formula: C13H13ClN2O2S
    5. Molecular Weight: 310.7991
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134141-09-6.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: ethyl 4-(2-chlorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4-(2-chlorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(134141-09-6)
    11. EPA Substance Registry System: ethyl 4-(2-chlorophenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(134141-09-6)

  • 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: 134141-09-6(Hazardous Substances Data)

134141-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134141-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,4 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134141-09:
(8*1)+(7*3)+(6*4)+(5*1)+(4*4)+(3*1)+(2*0)+(1*9)=86
86 % 10 = 6
So 134141-09-6 is a valid CAS Registry Number.

134141-09-6Relevant articles and documents

Larvicidal study of tetrahydropyrimidine scaffolds against Anopheles arabiensis and structural insight by single crystal X-ray studies

Bairagi, Keshab M.,Venugopala, Katharigatta N.,Mondal, Pradip Kumar,Gleiser, Raquel M.,Chopra, Deepak,García, Daniel,Odhav, Bharti,Nayak, Susanta K.

, p. 1924 - 1932 (2018)

A series of methyl or ethyl 4-(substitutedphenyl/pyridyl)-6-methyl-2-oxo/thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate (HPM) analogues 4a–g were synthesized and evaluated for larvicidal activity against Anopheles arabiensis. These newly synthesized co

Antidiabetic activity of dihydropyrimidine scaffolds and structural insight by single crystal x-ray studies

Alwassil, Osama I.,Bairagi, Keshab M.,Emeka, Promise Madu,Gonnade, Rajesh G.,Khalil, Hany Ezzat,Nayak, Susanta K.,Sangtani, Ekta,Venugopala, Katharigatta N.,Younis, Nancy Safwat

, p. 996 - 1003 (2020/08/19)

Background: This research project is designed to identify the anti-diabetic effects of the newly synthesized compounds to conclude the perspective of consuming one or more of these new synthetic compounds for diabetes management. Introduction: A series of

A reactant promoted solvent free synthesis of 3,4-dihydropyrimidin-2(1H)-thione analogues using ammonium thiocyanate

Khatri, Chetan K.,Potadar, Santoshkumar M.,Chaturbhuj, Ganesh U.

supporting information, p. 1778 - 1780 (2017/04/13)

This is the first-time ammonium thiocyanate (NH4SCN) has been used as a self-promoting reactant for the synthesis of 3,4-dihydropyrimidin-2(1H)-thiones. This report describes a greener, efficient and economic protocol for one pot three-component synthesis of Biginelli compounds using various aldehydes, β-ketoesters and ammonium thiocyanate. Ammonium thiocyanate being a weak acid, accelerate the rate of reaction to obtain Biginelli compounds in solvent-free condition at 110?°C. The key advantages of the present method are high yields, short reaction time, solvent free condition, easy workup and ability to tolerate a variety of functional groups. Ammonium thiocyanate is readily available, cheaper, safer and industrial acceptable material which gives economical as well as ecological rewards to the present method.

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