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869810-42-4

1-(tert-butyldimethylsilyloxy)-4-cyclohexyl-4-(tetrahydro-2H-pyran-2-yloxy)-but-2-yne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 869810-42-4 Structure

  • Basic information

    1. Product Name: 1-(tert-butyldimethylsilyloxy)-4-cyclohexyl-4-(tetrahydro-2H-pyran-2-yloxy)-but-2-yne
    2. Synonyms: 1-(tert-butyldimethylsilyloxy)-4-cyclohexyl-4-(tetrahydro-2H-pyran-2-yloxy)-but-2-yne
    3. CAS NO:869810-42-4
    4. Molecular Formula:
    5. Molecular Weight: 366.616
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 869810-42-4.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: 1-(tert-butyldimethylsilyloxy)-4-cyclohexyl-4-(tetrahydro-2H-pyran-2-yloxy)-but-2-yne(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(tert-butyldimethylsilyloxy)-4-cyclohexyl-4-(tetrahydro-2H-pyran-2-yloxy)-but-2-yne(869810-42-4)
    11. EPA Substance Registry System: 1-(tert-butyldimethylsilyloxy)-4-cyclohexyl-4-(tetrahydro-2H-pyran-2-yloxy)-but-2-yne(869810-42-4)

  • 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: 869810-42-4(Hazardous Substances Data)

869810-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869810-42-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,8,1 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 869810-42:
(8*8)+(7*6)+(6*9)+(5*8)+(4*1)+(3*0)+(2*4)+(1*2)=214
214 % 10 = 4
So 869810-42-4 is a valid CAS Registry Number.

869810-42-4Relevant articles and documents

Dynamic kinetic asymmetric allylic alkylations of allenes

Trost, Barry M.,Fandrick, Daniel R.,Dinh, Diana C.

, p. 14186 - 14187 (2007/10/03)

The dynamic kinetic asymmetric allylic alkylations of racemic allene acetates has been developed with the DACH-phenyl Trost ligand 2 to give general access to allenes with high enantiomeric excess (84-95%) for both malonate and amine nucleophiles. Further

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