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120353-58-4

N-PHENYL-2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120353-58-4 Structure

  • Basic information

    1. Product Name: N-PHENYL-2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE
    2. Synonyms: N-PHENYL-2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE;TOSLAB 725289
    3. CAS NO:120353-58-4
    4. Molecular Formula: C17H14N2OS
    5. Molecular Weight: 294.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120353-58-4.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: N-PHENYL-2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-PHENYL-2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE(120353-58-4)
    11. EPA Substance Registry System: N-PHENYL-2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE(120353-58-4)

  • 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: 120353-58-4(Hazardous Substances Data)

120353-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120353-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,5 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 120353-58:
(8*1)+(7*2)+(6*0)+(5*3)+(4*5)+(3*3)+(2*5)+(1*8)=84
84 % 10 = 4
So 120353-58-4 is a valid CAS Registry Number.

120353-58-4Relevant articles and documents

1-(cyanomethyl)benzotriazole as a convenient precursor for the synthesis of 2-substituted thiazoles

Katritzky,Chen,Yang

, p. 5638 - 5642 (2007/10/03)

Treatment of 1-(cyanomethyl)benzotriazole with hydrogen peroxide followed by a Lawesson reagent afforded (benzotriazol-1-yl)thioacetamide which condensed with α-halo carbonyl compounds (Hantzsch thiazole synthesis) to give the corresponding 2-(benzotriazol-1-ylmethyl)thiazoles. Lithiation of 2-(benzotriazol-1-ylmethyl)-4-phenylthiazole with butyllithium occurred exclusively at the methylene group, and subsequent quenching of the resulting anion with alkyl halides produced the corresponding alkylated products in good yields. Treatment of these intermediates with Grignard reagents in toluene or with electron-rich heterocycles in the presence of zinc bromide resulted in the displacement of benzotriazole to afford the corresponding thiazoles with elaborated 2-substituents.

Reactions with Monothiomalonamides: Synthesis of Polysubstituted Thiazoles

El-Reedy, A. M.,Hussain, S. M.,Youssef, M. M. M.

, p. 521 - 529 (2007/10/02)

Monothiomalonamides (1a, b) coupled with arenediazonium salts yield the α-arylhydrazone derivatives (2a-e).Reaction of 1a, b with α-haloketones afforded polysubstituted thiazoles 6a-e.Compounds 6 condensed with p-nitrosodimethylaniline and coupled with ar

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