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1041346-08-0

C18H28Se is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1041346-08-0 Structure

  • Basic information

    1. Product Name: C18H28Se
    2. Synonyms:
    3. CAS NO:1041346-08-0
    4. Molecular Formula:
    5. Molecular Weight: 323.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1041346-08-0.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: C18H28Se(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H28Se(1041346-08-0)
    11. EPA Substance Registry System: C18H28Se(1041346-08-0)

  • 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: 1041346-08-0(Hazardous Substances Data)

1041346-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041346-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,3,4 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1041346-08:
(9*1)+(8*0)+(7*4)+(6*1)+(5*3)+(4*4)+(3*6)+(2*0)+(1*8)=100
100 % 10 = 0
So 1041346-08-0 is a valid CAS Registry Number.

1041346-08-0Downstream Products

1041346-08-0Relevant articles and documents

A PhSeCl-mediated allylic oxidation of prenyl moiety: A convenient method for the construction of 3-isopenten-2-ol unit

Oshida, Motoko,Nakamura, Tomoaki,Nakazaki, Atsuo,Kobayashi, Susumu

, p. 404 - 406 (2008)

A phenylselenenyl chloride (PhSeCl)-mediated allylic oxidation to give allylically rearranged alcohol has been developed. A possible mechanism for the present reaction is generation of allylic selenide from prenyl moiety via [1,3]-sigmatropic rearrangement, followed by oxidation and [2,3]-sigmatropic rearrangement to afford 3-isopenten-2-ol.

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