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2-Propyl-5-(pyrimidin-5-yl)thiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1109226-43-8 Structure
  • Basic information

    1. Product Name: 2-Propyl-5-(pyrimidin-5-yl)thiazole
    2. Synonyms: 2-Propyl-5-(pyrimidin-5-yl)thiazole
    3. CAS NO:1109226-43-8
    4. Molecular Formula: C10H11N3S
    5. Molecular Weight: 205.27944
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1109226-43-8.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: 2-Propyl-5-(pyrimidin-5-yl)thiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propyl-5-(pyrimidin-5-yl)thiazole(1109226-43-8)
    11. EPA Substance Registry System: 2-Propyl-5-(pyrimidin-5-yl)thiazole(1109226-43-8)
  • 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: 1109226-43-8(Hazardous Substances Data)

1109226-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1109226-43-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,9,2,2 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1109226-43:
(9*1)+(8*1)+(7*0)+(6*9)+(5*2)+(4*2)+(3*6)+(2*4)+(1*3)=118
118 % 10 = 8
So 1109226-43-8 is a valid CAS Registry Number.

1109226-43-8Downstream Products

1109226-43-8Relevant articles and documents

Solvent-free palladium-catalyzed direct arylation of heteroaromatics with aryl bromides

Bensaid, Souhila,Doucet, Henri

experimental part, p. 1559 - 1567 (2012/10/08)

Solvent is one of the major sources of waste in the course of catalyzed direct arylations. Some palladium-catalyzed direct arylations of heteroaromatics can be advantageously performed without any solvent. In the presence of palladium catalysts (1 mol%) and potassium acetate as the base, the direct 5-arylation of some thiazoles, thiophenes, furans, or pyrroles with aryl bromides as coupling partners proceeds highly regioselectively and in moderate to high yields. However, the use of these solvent-free conditions is limited to electron-deficient aryl bromides. Copyright

Cyclopentyl methyl ether: An alternative solvent for palladium-catalyzed direct arylation of heteroaromatics

Beydoun, Kassem,Doucet, Henri

experimental part, p. 526 - 534 (2012/03/09)

Some ethers, such as cyclopentyl methyl ether and di-n-butyl ether, which can be considered as "greener" solvents than N,N-dimethylacetamide (DMAc) or DMF, can be advantageously employed for the palladium-catalyzed direct arylation of heteroaromatics. In the presence of such ethers and only 0.5-1 mol% of palladium catalysts at 125-150°C, the direct 5-arylation of thiazoles, thiophenes, or furans by using aryl bromides as coupling partners proceeds in moderate to high yields.

Palladium-catalysed direct arylations of heteroaromatics using more eco-compatible solvents pentan-1-ol or 3-methylbutan-1-ol

Bensaid, Souhila,Laidaoui, Nouria,El Abed, Douniazad,Kacimi, Soufi,Doucet, Henri

experimental part, p. 1383 - 1387 (2011/03/22)

The palladium-catalysed direct coupling of aryl halides with heteroaromatics in greener solvents than DMF or DMAc, which are often employed for such couplings, would be a considerable advantage for both industrial application and sustainable development.

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