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1581259-15-5

ethyl 2-[N-(4-chlorophenyl)-N-(p-tolyl)sulfamoyl]-2-diazoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1581259-15-5 Structure

  • Basic information

    1. Product Name: ethyl 2-[N-(4-chlorophenyl)-N-(p-tolyl)sulfamoyl]-2-diazoacetate
    2. Synonyms: ethyl 2-[N-(4-chlorophenyl)-N-(p-tolyl)sulfamoyl]-2-diazoacetate
    3. CAS NO:1581259-15-5
    4. Molecular Formula:
    5. Molecular Weight: 393.851
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1581259-15-5.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: ethyl 2-[N-(4-chlorophenyl)-N-(p-tolyl)sulfamoyl]-2-diazoacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-[N-(4-chlorophenyl)-N-(p-tolyl)sulfamoyl]-2-diazoacetate(1581259-15-5)
    11. EPA Substance Registry System: ethyl 2-[N-(4-chlorophenyl)-N-(p-tolyl)sulfamoyl]-2-diazoacetate(1581259-15-5)

  • 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: 1581259-15-5(Hazardous Substances Data)

1581259-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1581259-15-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,1,2,5 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1581259-15:
(9*1)+(8*5)+(7*8)+(6*1)+(5*2)+(4*5)+(3*9)+(2*1)+(1*5)=175
175 % 10 = 5
So 1581259-15-5 is a valid CAS Registry Number.

1581259-15-5Relevant articles and documents

Synthesis of benzo-γ-sultams via the Rh-catalyzed aromatic C-H functionalization of diazosulfonamides

Yang, Zhanhui,Xu, Jiaxi

, p. 3616 - 3618 (2014/04/03)

An efficient synthesis of 1-aryl-benzo-γ-sultams, 1-aryl-1,3-dihydrobenzo[c]isothiazole-2,2-dioxides, was achieved in 65-99% yields via the Rh-catalyzed intramolecular aromatic C-H functionalization of N,N-diaryl diazosulfonamides with 0.5 mol% Rh2(oct)4 as the catalyst. This journal is the Partner Organisations 2014.

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