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dimethyl benzothiophen-4,5-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100590-40-7

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  • 100590-40-7 Structure

  • Basic information

    1. Product Name: dimethyl benzothiophen-4,5-dicarboxylate
    2. Synonyms:
    3. CAS NO:100590-40-7
    4. Molecular Formula:
    5. Molecular Weight: 250.275
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: dimethyl benzothiophen-4,5-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl benzothiophen-4,5-dicarboxylate(100590-40-7)
    11. EPA Substance Registry System: dimethyl benzothiophen-4,5-dicarboxylate(100590-40-7)

  • 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: 100590-40-7(Hazardous Substances Data)

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100590-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100590-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,9 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100590-40:
(8*1)+(7*0)+(6*0)+(5*5)+(4*9)+(3*0)+(2*4)+(1*0)=77
77 % 10 = 7
So 100590-40-7 is a valid CAS Registry Number.

100590-40-7Downstream Products

100590-40-7Relevant academic research and scientific papers

CYCLOADDITION REACTIONS OF 2-VINYLTHIOPHEN

Abarca, Belen,Ballesteros, Rafael,Enriquez, Emilio,Jones, Gurnos

, p. 2435 - 2440 (2007/10/02)

Cycloaddition reactions between 2-vinylthiophen and the dienophiles maleic anhydride, dimethyl acetylenedicarboxylate, methyl propiolate, and methyl acrylate, are reported.Products include simple benzotiophen carboxylates (6, 13, 17) and reduced derivatives (3, 4, 18).The acetylenic dienophiles also gave a dihydrobenzthienyl-acrylate (16) or -fumarate (11), and the dithienylcyclohexene esters (7) and (14).

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