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1261036-06-9

C27H23NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1261036-06-9 Structure

  • Basic information

    1. Product Name: C27H23NO4
    2. Synonyms:
    3. CAS NO:1261036-06-9
    4. Molecular Formula:
    5. Molecular Weight: 425.484
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1261036-06-9.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: C27H23NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C27H23NO4(1261036-06-9)
    11. EPA Substance Registry System: C27H23NO4(1261036-06-9)

  • 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: 1261036-06-9(Hazardous Substances Data)

1261036-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1261036-06-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,0,3 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1261036-06:
(9*1)+(8*2)+(7*6)+(6*1)+(5*0)+(4*3)+(3*6)+(2*0)+(1*6)=109
109 % 10 = 9
So 1261036-06-9 is a valid CAS Registry Number.

1261036-06-9Downstream Products

1261036-06-9Relevant articles and documents

Copper-catalyzed tandem reactions of 1-(2-iodoary)-2-yn-1-ones with isocyanides for the synthesis of 4-oxo-indeno[1,2-b ]pyrroles

Cai, Qian,Zhou, Fengtao,Xu, Tianfeng,Fu, Liangbing,Ding, Ke

, p. 340 - 343 (2011)

A novel copper-catalyzed tandem reaction of 1-(2-iodoaryl)-2-yn-1-ones with isocyanides is described. The reaction is through a formal [3 + 2] cycloaddition/coupling tandem process and leads to efficient formation of 4-oxo-indeno[1,2-b]pyrroles.

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