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81467-57-4

3,5-di-butyl-1,2-benzoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81467-57-4 Structure

  • Basic information

    1. Product Name: 3,5-di-butyl-1,2-benzoquinone
    2. Synonyms: 3,5-di-butyl-1,2-benzoquinone
    3. CAS NO:81467-57-4
    4. Molecular Formula:
    5. Molecular Weight: 220.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81467-57-4.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: 3,5-di-butyl-1,2-benzoquinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-di-butyl-1,2-benzoquinone(81467-57-4)
    11. EPA Substance Registry System: 3,5-di-butyl-1,2-benzoquinone(81467-57-4)

  • 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: 81467-57-4(Hazardous Substances Data)

81467-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81467-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,6 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81467-57:
(7*8)+(6*1)+(5*4)+(4*6)+(3*7)+(2*5)+(1*7)=144
144 % 10 = 4
So 81467-57-4 is a valid CAS Registry Number.

81467-57-4Upstream product

81467-57-4Downstream Products

81467-57-4Relevant articles and documents

Bis(p-methoxyphenyl) Selenoxide as a Mild and Selective Oxidizing Agent

Ogura, Fumio,Yamaguchi, Hachiro,Otsubo, Tetsuo,Tanaka, Hiroyuki

, p. 641 - 642 (1982)

The title compound oxidized thiolsto disulfides, sulfides to sulfoxides, hydroquinone or catechol to benzoquinones, and phosphine to phosphine oxide in high yields under very mild conditions.In addition, it functioned as a useful reagent for the syntheses of 1,2,4-thiadiazole derivatives from thioureas or thioamides.

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