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1187186-13-5

1,4-bis(4-ethoxyphenyl)anthraquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1187186-13-5 Structure

  • Basic information

    1. Product Name: 1,4-bis(4-ethoxyphenyl)anthraquinone
    2. Synonyms: 1,4-bis(4-ethoxyphenyl)anthraquinone
    3. CAS NO:1187186-13-5
    4. Molecular Formula:
    5. Molecular Weight: 448.518
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1187186-13-5.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: 1,4-bis(4-ethoxyphenyl)anthraquinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-bis(4-ethoxyphenyl)anthraquinone(1187186-13-5)
    11. EPA Substance Registry System: 1,4-bis(4-ethoxyphenyl)anthraquinone(1187186-13-5)

  • 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: 1187186-13-5(Hazardous Substances Data)

1187186-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1187186-13-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,1,8 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1187186-13:
(9*1)+(8*1)+(7*8)+(6*7)+(5*1)+(4*8)+(3*6)+(2*1)+(1*3)=175
175 % 10 = 5
So 1187186-13-5 is a valid CAS Registry Number.

1187186-13-5Downstream Products

1187186-13-5Relevant articles and documents

Brominated thiophenes as precursors in the preparation of brominated and arylated anthraquinones

Thiemann, Thies,Tanaka, Yasuko,Iniesta, Jesus

experimental part, p. 1013 - 1031 (2009/10/10)

Brominated anthraquinones can be synthesized directly from bromothiophenes when these are reacted with 1,4-naphthoquinones in the presence of meta-chloroperoxybenzoic acid. The bromoanthraquinones are versatile building blocks in the preparation of arylated anthraquinones and of extended π-systems with interspersed anthraquinone units.

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