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CAS

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808739-72-2

6-[4-(tert-butyldimethylsilyloxy)phenyl]-4-[(4-methylphenyl)sulfonyl]hexan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 808739-72-2 Structure

  • Basic information

    1. Product Name: 6-[4-(tert-butyldimethylsilyloxy)phenyl]-4-[(4-methylphenyl)sulfonyl]hexan-2-one
    2. Synonyms: 6-[4-(tert-butyldimethylsilyloxy)phenyl]-4-[(4-methylphenyl)sulfonyl]hexan-2-one
    3. CAS NO:808739-72-2
    4. Molecular Formula:
    5. Molecular Weight: 460.71
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 808739-72-2.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: 6-[4-(tert-butyldimethylsilyloxy)phenyl]-4-[(4-methylphenyl)sulfonyl]hexan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-[4-(tert-butyldimethylsilyloxy)phenyl]-4-[(4-methylphenyl)sulfonyl]hexan-2-one(808739-72-2)
    11. EPA Substance Registry System: 6-[4-(tert-butyldimethylsilyloxy)phenyl]-4-[(4-methylphenyl)sulfonyl]hexan-2-one(808739-72-2)

  • 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: 808739-72-2(Hazardous Substances Data)

808739-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 808739-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,8,7,3 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 808739-72:
(8*8)+(7*0)+(6*8)+(5*7)+(4*3)+(3*9)+(2*7)+(1*2)=202
202 % 10 = 2
So 808739-72-2 is a valid CAS Registry Number.

808739-72-2Relevant articles and documents

First total synthesis of (±)-prelunularin

Comas, Horacio,Pandolfi, Enrique

, p. 2493 - 2498 (2007/10/03)

The first total synthesis of (±)-prelunularin is described employing an intramolecular aldol addition/sulfinate elimination tandem reaction. Investigations on the mechanism of the one-pot cyclization reaction using time-dependent NMR spectroscopy suggested that the sulfinate elimination took place before the intramolecular ring-closing aldol addition.

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