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1148110-34-2

7-{[1-(ethylsulfonyl)-4-piperidinyl]oxy}-6-phenylisoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1148110-34-2 Structure

  • Basic information

    1. Product Name: 7-{[1-(ethylsulfonyl)-4-piperidinyl]oxy}-6-phenylisoquinoline
    2. Synonyms: 7-{[1-(ethylsulfonyl)-4-piperidinyl]oxy}-6-phenylisoquinoline
    3. CAS NO:1148110-34-2
    4. Molecular Formula:
    5. Molecular Weight: 396.51
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1148110-34-2.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: 7-{[1-(ethylsulfonyl)-4-piperidinyl]oxy}-6-phenylisoquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-{[1-(ethylsulfonyl)-4-piperidinyl]oxy}-6-phenylisoquinoline(1148110-34-2)
    11. EPA Substance Registry System: 7-{[1-(ethylsulfonyl)-4-piperidinyl]oxy}-6-phenylisoquinoline(1148110-34-2)

  • 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: 1148110-34-2(Hazardous Substances Data)

1148110-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1148110-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,8,1,1 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1148110-34:
(9*1)+(8*1)+(7*4)+(6*8)+(5*1)+(4*1)+(3*0)+(2*3)+(1*4)=112
112 % 10 = 2
So 1148110-34-2 is a valid CAS Registry Number.

1148110-34-2Downstream Products

1148110-34-2Relevant articles and documents

Discovery of 6-aryl-7-alkoxyisoquinoline inhibitors of IκB kinase-β (IKK-β)

Christopher, John A.,Bamborough, Paul,Alder, Catherine,Campbell, Amanda,Cutler, Geoffrey J.,Down, Kenneth,Hamadi, Ahmed M.,Jolly, Adrian M.,Kerns, Jeffrey K.,Lucas, Fiona S.,Mellor, Geoffrey W.,Miller, David D.,Morse, Mary A.,Pancholi, Kiritkant D.,Rumsey, William,Solanke, Yemisi E.,Williamson, Rick

, p. 3098 - 3102 (2009)

The identification and progression of a potent and selective series of isoquinoline inhibitors of IκB kinase-β (IKK-β) are described. Hit-generation chemistry based on IKK-β active-site knowledge yielded a weakly potent but tractable chemotype that was rapidly progressed into a series with robust enzyme and cellular activity and significant selectivity over IKK-α.

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