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1019983-99-3

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

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  • 1019983-99-3 Structure

  • Basic information

    1. Product Name: dimethylanthradithiophene
    2. Synonyms:
    3. CAS NO:1019983-99-3
    4. Molecular Formula:
    5. Molecular Weight: 318.463
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1019983-99-3.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: dimethylanthradithiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethylanthradithiophene(1019983-99-3)
    11. EPA Substance Registry System: dimethylanthradithiophene(1019983-99-3)

  • 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: 1019983-99-3(Hazardous Substances Data)

1019983-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1019983-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,9,9,8 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1019983-99:
(9*1)+(8*0)+(7*1)+(6*9)+(5*9)+(4*8)+(3*3)+(2*9)+(1*9)=183
183 % 10 = 3
So 1019983-99-3 is a valid CAS Registry Number.

1019983-99-3Downstream Products

1019983-99-3Relevant articles and documents

Synthesis, physical properties, and field-effect mobility of isomerically pure syn -/ anti -anthradithiophene derivatives

Mamada, Masashi,Minamiki, Tsukuru,Katagiri, Hiroshi,Tokito, Shizuo

supporting information; experimental part, p. 4062 - 4065 (2012/09/22)

Isomerically pure syn-/anti-isomers of 2,8-dimethylanthradithiophene (DMADT) were synthesized in five steps and characterized using thermogravimetry, X-ray single crystal analysis, UV-vis absorption, and electrochemical measurements. The physical properties in solution were slightly different for each isomer, whereby the more obvious differences were observed in the solid state. A field-effect transistor using the anti-isomer showed a much higher performance than that using the syn-isomer.

Functionalized anthradithiophenes for organic field-effect transistors

Chen, Ming-Chou,Kim, Choongik,Chen, Sheng-Yu,Chiang, Yen-Ju,Chung, Ming-Che,Facchetti, Antonio,Marks, Tobin J.

experimental part, p. 1029 - 1036 (2009/05/07)

Two new semiconductors for organic thin-film transistors (OTFTs), diperfluorophenyl anthradithiophene (DFPADT) and dimethyl anthradithiophene (DMADT), have been synthesized and characterized. The first material exhibits ambipolar transport in OTFT devices

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