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4-bromo-5-iodo-2-tolylthiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393673-09-0 Structure
  • Basic information

    1. Product Name: 4-bromo-5-iodo-2-tolylthiazole
    2. Synonyms: 4-bromo-5-iodo-2-tolylthiazole
    3. CAS NO:1393673-09-0
    4. Molecular Formula:
    5. Molecular Weight: 380.047
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393673-09-0.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: 4-bromo-5-iodo-2-tolylthiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-bromo-5-iodo-2-tolylthiazole(1393673-09-0)
    11. EPA Substance Registry System: 4-bromo-5-iodo-2-tolylthiazole(1393673-09-0)
  • 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: 1393673-09-0(Hazardous Substances Data)

1393673-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393673-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,6,7 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1393673-09:
(9*1)+(8*3)+(7*9)+(6*3)+(5*6)+(4*7)+(3*3)+(2*0)+(1*9)=190
190 % 10 = 0
So 1393673-09-0 is a valid CAS Registry Number.

1393673-09-0Relevant articles and documents

Highly flexible π-expanded cyclooctatetraenes: Cyclic thiazole tetramers with head-to-tail connection

Mouri, Kazuhiro,Saito, Shohei,Yamaguchi, Shigehiro

supporting information; experimental part, p. 5971 - 5975 (2012/07/30)

Flipping fast: Head-to-tail cyclic thiazole tetramers representing flexible π-expanded cyclooctatetraenes were designed and synthesized (see picture). The presence of fused thiazole rings in a head-to-tail arrangement leads to a strong columnar stacking of the shallow saddle-shaped π-conjugated molecules, an unusually low inversion barrier of 6.8kcal mol-1, and reduction-induced complete planarization to an aromatic ring system. Copyright

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