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1092972-97-8

C19H28O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1092972-97-8 Structure

  • Basic information

    1. Product Name: C19H28O2
    2. Synonyms: C19H28O2
    3. CAS NO:1092972-97-8
    4. Molecular Formula:
    5. Molecular Weight: 288.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1092972-97-8.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: C19H28O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H28O2(1092972-97-8)
    11. EPA Substance Registry System: C19H28O2(1092972-97-8)

  • 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: 1092972-97-8(Hazardous Substances Data)

1092972-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1092972-97-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,9,7 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1092972-97:
(9*1)+(8*0)+(7*9)+(6*2)+(5*9)+(4*7)+(3*2)+(2*9)+(1*7)=188
188 % 10 = 8
So 1092972-97-8 is a valid CAS Registry Number.

1092972-97-8Downstream Products

1092972-97-8Relevant articles and documents

Tandem cross-metathesis/hydrogenation: application to an enantioselective synthesis of pentadecyl 6-hydroxydodecanoate

Bourcet, Emmanuel,Virolleaud, Marie-Alice,Fache, Fabienne,Piva, Olivier

, p. 6816 - 6818 (2008)

The synthesis of pentadecyl 6-hydroxydodecanoate, a component isolated from the leaves of Artabotrys odoratissimus, has been achieved through a tandem cross-metathesis/hydrogenation sequence. The enantioselective synthesis required first the preparation of a homoallylic alcohol obtained by a free-metal allyl transfer from a camphor derivative to heptanal.

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