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5-Chloro-2-(4-cyanophenyl)benzo[d]thiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17930-04-0 Structure
  • Basic information

    1. Product Name: 5-Chloro-2-(4-cyanophenyl)benzo[d]thiazole
    2. Synonyms: 5-Chloro-2-(4-cyanophenyl)benzo[d]thiazole
    3. CAS NO:17930-04-0
    4. Molecular Formula:
    5. Molecular Weight: 270.742
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17930-04-0.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: 5-Chloro-2-(4-cyanophenyl)benzo[d]thiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Chloro-2-(4-cyanophenyl)benzo[d]thiazole(17930-04-0)
    11. EPA Substance Registry System: 5-Chloro-2-(4-cyanophenyl)benzo[d]thiazole(17930-04-0)
  • 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: 17930-04-0(Hazardous Substances Data)

17930-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17930-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17930-04:
(7*1)+(6*7)+(5*9)+(4*3)+(3*0)+(2*0)+(1*4)=110
110 % 10 = 0
So 17930-04-0 is a valid CAS Registry Number.

17930-04-0Downstream Products

17930-04-0Relevant articles and documents

Urea nitrate–catalyzed C-N and C-S bond formation: A mechanochemical approach for 5-chloro-2-arylbenzo[d]thiazole derivatives

Sethiya, Ayushi,Sahiba, Nusrat,Soni, Jay,Agarwal, Shikha

, p. 873 - 881 (2021)

A series of substituted 5-chloro-2-arylbenzo[d]thiazoles were synthesized using 4-chloro-2-aminothiophenol and aromatic aldehydes in the presence of urea nitrate as a catalyst using the mechanochemical grindstone technique. This protocol was effectively carried out under metal-free conditions at room temperature, and the desired products were obtained in high to excellent yields in short reaction time (30–60 s). The structure of all the synthesized derivatives was confirmed by spectral characterization. The designed protocol has several benefits like eco-friendly, solvent-free, high yields, easy workup, and recyclability of catalyst. The catalyst was reusable at least four times without significant loss of activity. The good functional group tolerance with a series of derivatives has been demonstrated.

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