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1428362-13-3

C18H16N2O2S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428362-13-3 Structure

  • Basic information

    1. Product Name: C18H16N2O2S2
    2. Synonyms: C18H16N2O2S2
    3. CAS NO:1428362-13-3
    4. Molecular Formula:
    5. Molecular Weight: 356.469
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428362-13-3.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: C18H16N2O2S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H16N2O2S2(1428362-13-3)
    11. EPA Substance Registry System: C18H16N2O2S2(1428362-13-3)

  • 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: 1428362-13-3(Hazardous Substances Data)

1428362-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428362-13-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,3,6 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1428362-13:
(9*1)+(8*4)+(7*2)+(6*8)+(5*3)+(4*6)+(3*2)+(2*1)+(1*3)=153
153 % 10 = 3
So 1428362-13-3 is a valid CAS Registry Number.

1428362-13-3Relevant articles and documents

Palladium-catalyzed diarylmethyl C(sp3)-C(sp2) bond formation: A new coupling approach toward triarylmethanes

Xia, Ying,Hu, Fangdong,Liu, Zhenxing,Qu, Peiyuan,Ge, Rui,Ma, Chen,Zhang, Yan,Wang, Jianbo

, p. 1784 - 1787 (2013)

Palladium-catalyzed reductive coupling reactions between N-tosylhydrazones and aryl halides lead to the formation of C(sp3)-C(sp2) bonds. This approach provides a general route for the synthesis of triarylmethanes.

Synthesis of Di- and Triarylmethanes through Palladium-Catalyzed Reductive Coupling of N -Tosylhydrazones and Aryl Bromides

Xia, Yamu,Hu, Fangdong,Xia, Ying,Liu, Zhenxing,Ye, Fei,Zhang, Yan,Wang, Jianbo

, p. 1073 - 1086 (2017/02/24)

A palladium-catalyzed reductive coupling between N-tosylhydrazones and aryl bromides has been developed. The reaction provides an efficient method for the synthesis of diarylmethanes and triarylmethanes via the formation of C(sp2)-C(sp3) single bonds. This new methodology for the synthesis of diarylmethanes and triarylmethanes is featured by the ready availability of the starting materials, mild reaction conditions, and the tolerance of wide range of functional groups. The reaction follows a pathway including palladium carbene formation, migratory insertion, and reduction of the alkylpalladium(II) intermediate.

Synthesis of terminal allenes through copper-mediated cross-coupling of ethyne with N-tosylhydrazones or α-diazoesters

Ye, Fei,Wang, Chengpeng,Ma, Xiaoshen,Hossain, Mohammad Lokman,Xia, Ying,Zhang, Yan,Wang, Jianbo

, p. 647 - 652 (2016/09/12)

Ethyne is employed as coupling partner in coppermediated cross-coupling reactions with N-tosylhydrazones and α-diazoacetate, leading to the development of a new synthetic method for terminal allenes. With this novel coupling method, the terminal allenes w

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