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855871-30-6

2,3-dibromo-5,6-dimethoxy-[1,4]benzoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 855871-30-6 Structure

  • Basic information

    1. Product Name: 2,3-dibromo-5,6-dimethoxy-[1,4]benzoquinone
    2. Synonyms:
    3. CAS NO:855871-30-6
    4. Molecular Formula:
    5. Molecular Weight: 325.941
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 855871-30-6.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: 2,3-dibromo-5,6-dimethoxy-[1,4]benzoquinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-dibromo-5,6-dimethoxy-[1,4]benzoquinone(855871-30-6)
    11. EPA Substance Registry System: 2,3-dibromo-5,6-dimethoxy-[1,4]benzoquinone(855871-30-6)

  • 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: 855871-30-6(Hazardous Substances Data)

855871-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 855871-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,8,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 855871-30:
(8*8)+(7*5)+(6*5)+(5*8)+(4*7)+(3*1)+(2*3)+(1*0)=206
206 % 10 = 6
So 855871-30-6 is a valid CAS Registry Number.

855871-30-6Downstream Products

855871-30-6Relevant articles and documents

Photochromic coenzyme Q derivatives: Switching redox potentials with light

Simeth, Nadja A.,Kneuttinger, Andrea C.,Sterner, Reinhard,K?nig, Burkhard

, p. 6474 - 6483 (2017)

Coenzyme Q is an important redox cofactor involved in a variety of cellular processes, and is thus found in several cell compartments. We report a photochromic derivative of coenzyme Q that combines the molecular structures of the redox active cofactor and a photochromic dye. Light irradiation triggers an electronic rearrangement reversibly changing the redox potential. We used this effect to control the intermolecular redox reaction of the photochromic coenzyme Q derivative with dihydropyridine in solution by light irradiation. On mitochondria, the altered redox properties showed an effect on the respiratory chain. The experiments demonstrate that the redox reactions can be initiated inside the system of interest through irradiation with light and the accompanied photoisomerization.

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