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1000029-32-2

5-(4-chlorophenyl)-2-(4-methylphenyl)thiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1000029-32-2 Structure

  • Basic information

    1. Product Name: 5-(4-chlorophenyl)-2-(4-methylphenyl)thiazole
    2. Synonyms: 5-(4-chlorophenyl)-2-(4-methylphenyl)thiazole
    3. CAS NO:1000029-32-2
    4. Molecular Formula:
    5. Molecular Weight: 285.797
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1000029-32-2.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: 5-(4-chlorophenyl)-2-(4-methylphenyl)thiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(4-chlorophenyl)-2-(4-methylphenyl)thiazole(1000029-32-2)
    11. EPA Substance Registry System: 5-(4-chlorophenyl)-2-(4-methylphenyl)thiazole(1000029-32-2)

  • 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: 1000029-32-2(Hazardous Substances Data)

1000029-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1000029-32-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,0,2 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1000029-32:
(9*1)+(8*0)+(7*0)+(6*0)+(5*0)+(4*2)+(3*9)+(2*3)+(1*2)=52
52 % 10 = 2
So 1000029-32-2 is a valid CAS Registry Number.

1000029-32-2Downstream Products

1000029-32-2Relevant articles and documents

Programmed synthesis of arylthiazoles through sequential C-H couplings

Tani, Satoshi,Uehara, Takahiro N.,Yamaguchi, Junichiro,Itami, Kenichiro

, p. 123 - 135 (2014/01/06)

A programmed synthesis of privileged arylthiazoles via sequential C-H couplings catalyzed by palladium or nickel catalysts has been accomplished. This versatile protocol can supply all possible arylthiazole substitution patterns (2-aryl, 4-aryl, 5-aryl, 2

Direct arylation of thiazoles on water

Turner, Gemma L.,Morris, James A.,Greaney, Michael F.

, p. 7996 - 8000 (2008/09/17)

Wetter is better: The direct arylation of thiazoles on water is quicker, cleaner, and higher-yielding than arylation in organic solvents. The reaction works under mild conditions for an array of aryl iodides, producing 2,5-diaryl thiazoles in excellent yields. Importantly, novel bi-heteroaryl compounds are produced without the requirement for stoichiometric organometallic coupling agents. (Figure Presented).

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