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CAS

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172841-59-7

6-(benzyloxy)-1-phenylhex-4-yn-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 172841-59-7 Structure

  • Basic information

    1. Product Name: 6-(benzyloxy)-1-phenylhex-4-yn-1-one
    2. Synonyms: 6-(benzyloxy)-1-phenylhex-4-yn-1-one
    3. CAS NO:172841-59-7
    4. Molecular Formula:
    5. Molecular Weight: 278.351
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 172841-59-7.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-(benzyloxy)-1-phenylhex-4-yn-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(benzyloxy)-1-phenylhex-4-yn-1-one(172841-59-7)
    11. EPA Substance Registry System: 6-(benzyloxy)-1-phenylhex-4-yn-1-one(172841-59-7)

  • 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: 172841-59-7(Hazardous Substances Data)

172841-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172841-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,8,4 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 172841-59:
(8*1)+(7*7)+(6*2)+(5*8)+(4*4)+(3*1)+(2*5)+(1*9)=147
147 % 10 = 7
So 172841-59-7 is a valid CAS Registry Number.

172841-59-7Relevant articles and documents

Gold-Catalyzed Cycloisomerization and Diels-Alder Reaction of 1,6-Diyne Esters with Alkenes and Diazenes to Hydronaphthalenes and -cinnolines

Yan, Jianming,Tay, Guan Liang,Neo, Cuien,Lee, Bo Ra,Chan, Philip Wai Hong

supporting information, p. 4176 - 4179 (2015/09/15)

A method for the efficient preparation of hydronaphthalene and -cinnoline derivatives by Au(I)-catalyzed cycloisomerzation of 1,6-diyne esters followed by a Diels-Alder reaction with alkenes or diazenes under mild conditions at room temperature with catal

Enantioselective preparation of 8-oxabicyclo[3.2.1]octane derivatives via asymmetric [3+2]-cycloaddition of platinum-containing carbonyl ylides with vinyl ethers

Ishida, Kento,Kusama, Hiroyuki,Iwasawa, Nobuharu

supporting information; experimental part, p. 8842 - 8843 (2010/08/21)

A catalytic asymmetric synthesis of 8-oxabicyclo[3.2.1]octane derivatives was achieved through the [3+2]-cycloaddition of the platinum-containing carbonyl ylides generated from acyclic γ,δ-ynones on treatment with 10 mol % of PtCl2-Walphos and

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