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(3,4-dimethoxyphenyl)(4,5-dimethylthiazol-2-yl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609542-99-5 Structure
  • Basic information

    1. Product Name: (3,4-dimethoxyphenyl)(4,5-dimethylthiazol-2-yl)methanone
    2. Synonyms: (3,4-dimethoxyphenyl)(4,5-dimethylthiazol-2-yl)methanone
    3. CAS NO:1609542-99-5
    4. Molecular Formula:
    5. Molecular Weight: 277.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609542-99-5.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: (3,4-dimethoxyphenyl)(4,5-dimethylthiazol-2-yl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3,4-dimethoxyphenyl)(4,5-dimethylthiazol-2-yl)methanone(1609542-99-5)
    11. EPA Substance Registry System: (3,4-dimethoxyphenyl)(4,5-dimethylthiazol-2-yl)methanone(1609542-99-5)
  • 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: 1609542-99-5(Hazardous Substances Data)

1609542-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609542-99-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,5,4 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1609542-99:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*4)+(3*2)+(2*9)+(1*9)=185
185 % 10 = 5
So 1609542-99-5 is a valid CAS Registry Number.

1609542-99-5Downstream Products

1609542-99-5Relevant articles and documents

Direct C-2 acylation of thiazoles with aldehydes via metal- and solvent-free c-h activation in the presence of tert-butyl hydroperoxide

Khemnar, Ashok B.,Bhanage, Bhalchandra M.

, p. 110 - 114 (2014)

A novel and efficient methodology for the synthesis of heteroaryl ketones by C-H activation of aldehydes and thiazoles is developed. The reaction occurs smoothly, under metal-, acid- and solvent-free conditions using tert-butyl hydroperoxide as the oxidant under an air atmosphere, to afford a wide range of heteroaryl ketones in moderate to good yields. The sp2 C-H bonds in the aldehyde and thiazole undergo direct oxidative cross-coupling, resulting in C-2 acylation of the azole. Georg Thieme Verlag Stuttgart · New York.

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