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1092454-10-8

4-(benzyloxy)-1-phenylbutane-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1092454-10-8 Structure

  • Basic information

    1. Product Name: 4-(benzyloxy)-1-phenylbutane-1,3-dione
    2. Synonyms: 4-(benzyloxy)-1-phenylbutane-1,3-dione
    3. CAS NO:1092454-10-8
    4. Molecular Formula:
    5. Molecular Weight: 268.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1092454-10-8.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: 4-(benzyloxy)-1-phenylbutane-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(benzyloxy)-1-phenylbutane-1,3-dione(1092454-10-8)
    11. EPA Substance Registry System: 4-(benzyloxy)-1-phenylbutane-1,3-dione(1092454-10-8)

  • 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: 1092454-10-8(Hazardous Substances Data)

1092454-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1092454-10-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,4,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1092454-10:
(9*1)+(8*0)+(7*9)+(6*2)+(5*4)+(4*5)+(3*4)+(2*1)+(1*0)=138
138 % 10 = 8
So 1092454-10-8 is a valid CAS Registry Number.

1092454-10-8Relevant articles and documents

Ru-Catalyzed Chemo- and Enantioselective Hydrogenation of β-Diketones Assisted by the Neighboring Heteroatoms

Li, Wanfang,Lu, Bin,Xie, Xiaomin,Zhang, Zhaoguo

, p. 5509 - 5513 (2019)

A highly chemo- and enantioselective hydrogenation of β-diketones was achieved by using [Ru(benzene)(S)-SunPhosCl]Cl for consistency in THF. The neighboring heteroatoms played important roles in guaranteeing the reactivity and controlling the chemoselectivity. These results suggested a potential approach for the clean and facile synthesis of functionalized chiral β-hydroxy ketones, which could otherwise be prepared through much less step-economic transformations.

Chelation control in the [3+3] annulation reaction of alkoxy-substituted 1,1-diacylcyclopropanes with 1,3-bis(trimethylsilyloxy)-1,3-butadienes. Diversity-oriented synthesis of isochromanes

Karapetyan, Vahuni,Mkrtchyan, Satenik,Hefner, Jennifer,Fischer, Christine,Langer, Peter

supporting information; experimental part, p. 809 - 814 (2010/04/28)

(Chemical Equation Presented) Functionalized arenes were prepared by chelation-controlled [3 + 3] cyclization/cyclopropane opening reactions of 1-trimethylsilyloxy-1,3-butadienes with benzyloxy- or methoxy-substituted 1,1-diacylcyclopropanes. A number of benzyloxy-substituted derivatives were transformed into isochromanes by deprotection and subsequent cyclization. Mixed chromanes-isochromanes were prepared starting with 1,3-bis(silyloxy)-1,3- butadienes containing a remote chloride group. 2010 American Chemical Society.

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