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CAS

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36710-70-0

1-(4-nitrophenyl)isoquinoline N-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36710-70-0 Structure

  • Basic information

    1. Product Name: 1-(4-nitrophenyl)isoquinoline N-oxide
    2. Synonyms: 1-(4-nitrophenyl)isoquinoline N-oxide
    3. CAS NO:36710-70-0
    4. Molecular Formula:
    5. Molecular Weight: 266.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36710-70-0.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: 1-(4-nitrophenyl)isoquinoline N-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-nitrophenyl)isoquinoline N-oxide(36710-70-0)
    11. EPA Substance Registry System: 1-(4-nitrophenyl)isoquinoline N-oxide(36710-70-0)

  • 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: 36710-70-0(Hazardous Substances Data)

36710-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36710-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,1 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36710-70:
(7*3)+(6*6)+(5*7)+(4*1)+(3*0)+(2*7)+(1*0)=110
110 % 10 = 0
So 36710-70-0 is a valid CAS Registry Number.

36710-70-0Downstream Products

36710-70-0Relevant articles and documents

Regioselective decarboxylative cross-coupling of carboxy isoquinoline N -oxides

Rouchet, Jean-Baptiste E. Y.,Schneider, Cédric,Fruit, Corinne,Hoarau, Christophe

, p. 5919 - 5927 (2015)

A straightforward method for direct decarboxylative arylation of 1- and 3-carboxy isoquinaldic acid N-oxides with aryl iodides is reported. The reaction proceeded selectively at the carboxy function site to exclusively give the corresponding C-1/sub

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