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16112-22-4

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  • 16112-22-4 Structure

  • Basic information

    1. Product Name: 2-(4-methylphenyl)-5-phenylthiazole
    2. Synonyms: 2-(4-methylphenyl)-5-phenylthiazole
    3. CAS NO:16112-22-4
    4. Molecular Formula:
    5. Molecular Weight: 251.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16112-22-4.mol
    9. Article Data: 3

  • 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: 2-(4-methylphenyl)-5-phenylthiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-methylphenyl)-5-phenylthiazole(16112-22-4)
    11. EPA Substance Registry System: 2-(4-methylphenyl)-5-phenylthiazole(16112-22-4)

  • 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: 16112-22-4(Hazardous Substances Data)

16112-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16112-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,1 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16112-22:
(7*1)+(6*6)+(5*1)+(4*1)+(3*2)+(2*2)+(1*2)=64
64 % 10 = 4
So 16112-22-4 is a valid CAS Registry Number.

16112-22-4Relevant articles and documents

Cu-Catalyzed Aerobic Oxidative Sulfuration/Annulation Approach to Thiazoles via Multiple Csp3-H Bond Cleavage

Wang, Xiaoyang,Qiu, Xu,Wei, Jialiang,Liu, Jianzhong,Song, Song,Wang, Wen,Jiao, Ning

supporting information, p. 2632 - 2636 (2018/05/22)

A novel and practical Cu-catalyzed aerobic oxidative synthesis of thiazoles was developed. This chemistry for the first time achieved thiazole construction from simple aldehydes, amines, and element sulfur through multiple Csp3-H bond cleavage processes. Molecular oxygen was used as a green oxidant in this oxidative protocol. The substrate scope is broad with the tolerance of aliphatic amines. The mechanistic study might promote the reaction design for a new sulfuration/annulation reaction with readily available element sulfur.

Programmed synthesis of arylthiazoles through sequential C-H couplings

Tani, Satoshi,Uehara, Takahiro N.,Yamaguchi, Junichiro,Itami, Kenichiro

, p. 123 - 135 (2014/01/06)

A programmed synthesis of privileged arylthiazoles via sequential C-H couplings catalyzed by palladium or nickel catalysts has been accomplished. This versatile protocol can supply all possible arylthiazole substitution patterns (2-aryl, 4-aryl, 5-aryl, 2

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