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CAS

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145802-01-3

1-benzyl-9,9-dimethyl-4,5,6,8,9,10-hexahydrocyclooctapyridine-2,7(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145802-01-3 Structure

  • Basic information

    1. Product Name: 1-benzyl-9,9-dimethyl-4,5,6,8,9,10-hexahydrocyclooctapyridine-2,7(1H,3H)-dione
    2. Synonyms: 1-benzyl-9,9-dimethyl-4,5,6,8,9,10-hexahydrocyclooctapyridine-2,7(1H,3H)-dione
    3. CAS NO:145802-01-3
    4. Molecular Formula:
    5. Molecular Weight: 311.424
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145802-01-3.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-benzyl-9,9-dimethyl-4,5,6,8,9,10-hexahydrocyclooctapyridine-2,7(1H,3H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-9,9-dimethyl-4,5,6,8,9,10-hexahydrocyclooctapyridine-2,7(1H,3H)-dione(145802-01-3)
    11. EPA Substance Registry System: 1-benzyl-9,9-dimethyl-4,5,6,8,9,10-hexahydrocyclooctapyridine-2,7(1H,3H)-dione(145802-01-3)

  • 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: 145802-01-3(Hazardous Substances Data)

145802-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145802-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,8,0 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 145802-01:
(8*1)+(7*4)+(6*5)+(5*8)+(4*0)+(3*2)+(2*0)+(1*1)=113
113 % 10 = 3
So 145802-01-3 is a valid CAS Registry Number.

145802-01-3Downstream Products

145802-01-3Relevant articles and documents

Intramolecular [2+2] photocycloaddition of N-alkenoyl β - enaminones

Amougay, Aicha,Pete, Jean-Pierre,Piva, Olivier

, p. 7347 - 7350 (1992)

Intramolecular cycloaddition of N-alkenoyl β-enaminones occurs with high regioselectivity and diastereoselectivity leading to interesting synthons for the total synthesis of triquinanes or various sesquiterpenes.

Intramolecular [2 + 2] photocvcloaddition of N-alkenovl-β-enaminones

Amougay, Aicha,Pete, Jean-Pierre,Piva, Olivier

, p. 625 - 635 (2007/10/03)

The photolysis of cyclic N-alkenoyl β-enaminones is described. In general, a very regio- and stereoselective intramolecular [2 + 2] photocydoaddition was observed. The limitations of the reaction process are discussed. The main competitive reaction, which

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