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10562-66-0

1,1,4,4-Tetracyclohexyl-but-2-yne-1,4-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10562-66-0 Structure

  • Basic information

    1. Product Name: 1,1,4,4-Tetracyclohexyl-but-2-yne-1,4-diol
    2. Synonyms:
    3. CAS NO:10562-66-0
    4. Molecular Formula:
    5. Molecular Weight: 414.672
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10562-66-0.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: 1,1,4,4-Tetracyclohexyl-but-2-yne-1,4-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,4,4-Tetracyclohexyl-but-2-yne-1,4-diol(10562-66-0)
    11. EPA Substance Registry System: 1,1,4,4-Tetracyclohexyl-but-2-yne-1,4-diol(10562-66-0)

  • 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: 10562-66-0(Hazardous Substances Data)

10562-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10562-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10562-66:
(7*1)+(6*0)+(5*5)+(4*6)+(3*2)+(2*6)+(1*6)=80
80 % 10 = 0
So 10562-66-0 is a valid CAS Registry Number.

10562-66-0Downstream Products

10562-66-0Relevant articles and documents

Direct Exploitation of the Ethynyl Moiety in Calcium Carbide Through Sealed Ball Milling

Hosseini, Abolfazl,Schreiner, Peter R.

, p. 4339 - 4346 (2020)

Ball milling of calcium carbide (CaC2) enables the reaction of its ethynyl moiety with organic electrophiles. This was realized simply by co-milling CaC2 with organic substrates in a sealed jar without the need for an additive or a catalyst. Various ketones including those bearing α-hydrogens were ethynylated in good yields at short reaction times. Aryl halides are also amenable substrates for this protocol as they furnish aryl ethynes through a benzyne intermediate. This method offers a practical and cheap alternative to the established procedures for introducing ethynyl functionalities.

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