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455938-16-6

O-ethyl S-(1-tosylpiperidin-4-yl) carbonodithioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 455938-16-6 Structure

  • Basic information

    1. Product Name: O-ethyl S-(1-tosylpiperidin-4-yl) carbonodithioate
    2. Synonyms: O-ethyl S-(1-tosylpiperidin-4-yl) carbonodithioate
    3. CAS NO:455938-16-6
    4. Molecular Formula:
    5. Molecular Weight: 359.535
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 455938-16-6.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: O-ethyl S-(1-tosylpiperidin-4-yl) carbonodithioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: O-ethyl S-(1-tosylpiperidin-4-yl) carbonodithioate(455938-16-6)
    11. EPA Substance Registry System: O-ethyl S-(1-tosylpiperidin-4-yl) carbonodithioate(455938-16-6)

  • 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: 455938-16-6(Hazardous Substances Data)

455938-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 455938-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,5,9,3 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 455938-16:
(8*4)+(7*5)+(6*5)+(5*9)+(4*3)+(3*8)+(2*1)+(1*6)=186
186 % 10 = 6
So 455938-16-6 is a valid CAS Registry Number.

455938-16-6Relevant articles and documents

Substituted allyl diphenylphosphine oxides as radical allylating agents

Ouvry, Gilles,Quiclet-Sire, Beatrice,Zard, Samir Z.

, p. 5002 - 5006 (2006)

(Chemical Equation Presented) Radically useful: The radical addition of dithiocarbonates to branched allyl diphenylphosphine oxides can be followed by elimination of a diphenylphosphinoyl radical, thereby giving rise to allylated products (see scheme; Phth = phthalimido). Highly functionalized structures can thus be rapidly assembled under mild conditions and from cheap and readily available substrates and reagents.

A Convergent Radical Based Route to Trifluoromethyl Ketones and to α,β-Unsaturated Trifluoromethyl Ketones

Anthore, Lucile,Zard, Samir Z.

supporting information, p. 3058 - 3061 (2015/06/30)

A convergent synthesis of trifluoromethyl ketones and α,β-unsaturated trifluoromethyl ketones is described, starting with aliphatic iodides and dithiocarbonates (xanthates) and exploiting both the α- and β-fragmentations of a sulfonyl radical. The transfo

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