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1,5-dichloro-9,10-bis(5-methyl-2-thienyl)-9,10-dihydro-9,10-anthracenediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 223772-56-3 Structure
  • Basic information

    1. Product Name: 1,5-dichloro-9,10-bis(5-methyl-2-thienyl)-9,10-dihydro-9,10-anthracenediol
    2. Synonyms: 1,5-dichloro-9,10-bis(5-methyl-2-thienyl)-9,10-dihydro-9,10-anthracenediol
    3. CAS NO:223772-56-3
    4. Molecular Formula: C24H18Cl2O2S2
    5. Molecular Weight: 473.43452
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 223772-56-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,5-dichloro-9,10-bis(5-methyl-2-thienyl)-9,10-dihydro-9,10-anthracenediol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-dichloro-9,10-bis(5-methyl-2-thienyl)-9,10-dihydro-9,10-anthracenediol(223772-56-3)
    11. EPA Substance Registry System: 1,5-dichloro-9,10-bis(5-methyl-2-thienyl)-9,10-dihydro-9,10-anthracenediol(223772-56-3)
  • 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: 223772-56-3(Hazardous Substances Data)

223772-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223772-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,7,7 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 223772-56:
(8*2)+(7*2)+(6*3)+(5*7)+(4*7)+(3*2)+(2*5)+(1*6)=133
133 % 10 = 3
So 223772-56-3 is a valid CAS Registry Number.

223772-56-3Downstream Products

223772-56-3Relevant articles and documents

A novel acid-catalyzed rearrangement of 9,10-diaryl-9,10- dihydroanthracene-9,10-diols affording 10,10'-diaryl-9-anthrones

Smet, Mario,Van Dijk, Joachim,Dehaen, Wim

, p. 7859 - 7874 (2007/10/03)

Usually, 9,10-diarylanthracenes can be obtained by reduction of the corresponding 9,10-diaryl-9,10-dihydroanthracene-9,10-diols with Kl/NaH2PO2 in acetic acid. In contrast, we found that in case of heteroaromatic aryl substituents and when peri substituents are present on the anthracene residue, high amounts of anthrones are formed. These anthrones can be considered to result from a vinylogous pinacol rearrangement of the initial diol. To the best of our knowledge, this type of rearrangement is rarely observed, and the 10,10'-diaryl-9-anthrones obtained in this way, are difficult to prepare otherwise. We prepared a number of such compounds and studied the mechanism of the transformation involved. The results are in agreement with a bridged transition state 10.

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