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(2R)-1-(tert-butyldiphenylsilanyloxy)-6-(tetrahydropyran-2-yloxy)hex-4-yn-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 478800-17-8 Structure
  • Basic information

    1. Product Name: (2R)-1-(tert-butyldiphenylsilanyloxy)-6-(tetrahydropyran-2-yloxy)hex-4-yn-2-ol
    2. Synonyms: (2R)-1-(tert-butyldiphenylsilanyloxy)-6-(tetrahydropyran-2-yloxy)hex-4-yn-2-ol
    3. CAS NO:478800-17-8
    4. Molecular Formula:
    5. Molecular Weight: 452.666
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 478800-17-8.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: (2R)-1-(tert-butyldiphenylsilanyloxy)-6-(tetrahydropyran-2-yloxy)hex-4-yn-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R)-1-(tert-butyldiphenylsilanyloxy)-6-(tetrahydropyran-2-yloxy)hex-4-yn-2-ol(478800-17-8)
    11. EPA Substance Registry System: (2R)-1-(tert-butyldiphenylsilanyloxy)-6-(tetrahydropyran-2-yloxy)hex-4-yn-2-ol(478800-17-8)
  • 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: 478800-17-8(Hazardous Substances Data)

478800-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478800-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,8,0 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 478800-17:
(8*4)+(7*7)+(6*8)+(5*8)+(4*0)+(3*0)+(2*1)+(1*7)=178
178 % 10 = 8
So 478800-17-8 is a valid CAS Registry Number.

478800-17-8Relevant articles and documents

Total synthesis of (-)-histrionicotoxin 285A and (-)- perhydrohistrionicotoxin

Macdonald, James M.,Horsley, Helen T.,Ryan, John H.,Saubern, Simon,Holmes, Andrew B.

supporting information; experimental part, p. 4227 - 4229 (2009/06/06)

(Chemical Equation Presented) Starting from commercially available (S)-glycidol, and via a common intermediate, the total synthesis of (-)-histrionicotoxin 285A and (-)-perhydrohistrionicotoxin has been achieved. Key to this synthesis was the efficient co

Oxabicyclo[3.2.1]oct-6-enes as templates for the stereoselective synthesis of polypropionates: Total synthesis of callystatin a and C19-epi-callystatin A

Lautens, Mark,Stammers, Timothy A.

, p. 1993 - 2012 (2007/10/03)

The total synthesis of the polyketide natural product callystatin A and its novel analog C19-epi-callystatin A is described. Our strategy features the use of an enantiomerically pure oxabicyclo[3.2.1]oct-6-ene as a template for the stereocontrolled preparation of the C15-C21 polypropionate region.

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