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200403-55-0

3-methyl-N-(1,3-thiazol-2-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 200403-55-0 Structure

  • Basic information

    1. Product Name: 3-methyl-N-(1,3-thiazol-2-yl)benzamide
    2. Synonyms: Benzamide, 3-methyl-N-2-thiazolyl-;3-methyl-N-(1,3-thiazol-2-yl)benzamide
    3. CAS NO:200403-55-0
    4. Molecular Formula: C11H10N2OS
    5. Molecular Weight: 218.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 200403-55-0.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: 3-methyl-N-(1,3-thiazol-2-yl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methyl-N-(1,3-thiazol-2-yl)benzamide(200403-55-0)
    11. EPA Substance Registry System: 3-methyl-N-(1,3-thiazol-2-yl)benzamide(200403-55-0)

  • 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: 200403-55-0(Hazardous Substances Data)

200403-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 200403-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,4,0 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 200403-55:
(8*2)+(7*0)+(6*0)+(5*4)+(4*0)+(3*3)+(2*5)+(1*5)=60
60 % 10 = 0
So 200403-55-0 is a valid CAS Registry Number.

200403-55-0Downstream Products

200403-55-0Relevant articles and documents

N-(thiazol-2-yl)benzamide derivatives as a new series of supramolecular gelators: Role of methyl functionality and S?O interaction

Yadav, Priyanka,Ballabh, Amar

, (2019/11/13)

A new series of N-(thiazol-2-yl) benzamide derivatives were synthesized, characterized and investigated for their gelation behavior with the aim to elucidate the role of methyl functionality and multiple non-covalent interactions on gelation/non-gelation

Aminothiazoles and aminothiadiazoles as nucleophiles in aminocarbonylation of iodobenzene derivatives

Gergely, Máté,Kollár, László

, p. 2030 - 2040 (2018/03/21)

Various 2-, 3- and 4-substituted iodobenzenes were aminocarbonylated using aminothiazole and aminothiadiazole derivatives in palladium-catalysed reaction. The reaction is chemospecific toward the corresponding carboxamides. Consequently, the application o

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