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CAS

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1401828-69-0

3-benzoyl-1,2-bis(4-methoxyphenyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1401828-69-0 Structure

  • Basic information

    1. Product Name: 3-benzoyl-1,2-bis(4-methoxyphenyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde
    2. Synonyms: 3-benzoyl-1,2-bis(4-methoxyphenyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde
    3. CAS NO:1401828-69-0
    4. Molecular Formula:
    5. Molecular Weight: 511.577
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1401828-69-0.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: 3-benzoyl-1,2-bis(4-methoxyphenyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-benzoyl-1,2-bis(4-methoxyphenyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde(1401828-69-0)
    11. EPA Substance Registry System: 3-benzoyl-1,2-bis(4-methoxyphenyl)pyrrolo[1,2-a]quinoline-4-carbaldehyde(1401828-69-0)

  • 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: 1401828-69-0(Hazardous Substances Data)

1401828-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401828-69-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,8,2 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1401828-69:
(9*1)+(8*4)+(7*0)+(6*1)+(5*8)+(4*2)+(3*8)+(2*6)+(1*9)=140
140 % 10 = 0
So 1401828-69-0 is a valid CAS Registry Number.

1401828-69-0Downstream Products

1401828-69-0Relevant articles and documents

Palladium-catalyzed regioselective [3 + 2] annulation of internal alkynes and iodo-pyranoquinolines with concomitant ring opening

Aggarwal, Trapti,Jha, Rajeev R.,Tiwari, Rakesh K.,Kumar, Sonu,Kotla, Siva K. Reddy,Kumar, Sushil,Verma, Akhilesh K.

, p. 5184 - 5187,4 (2012)

A regioselective tandem synthesis of highly functionalized pyrrolo[1,2-a]quinolines has been developed through a novel strategy by palladium-catalyzed [3 + 2] annulation of iodo-pyranoquinolines and internal alkynes with subsequent ring opening. Pyranoquinoline with n-alkyl substitution at the 3-position leads to the formation of pyrrolo-acridones via [3 + 2] annulations/ring opening and successive intramolecular cross-aldol condensation.

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