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1026866-29-4

4-(3-oxo-1-phenyl-3-thiophen-2-yl-propyl)-3,4-dihydro-1H-benzo[b]azepine-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1026866-29-4 Structure

  • Basic information

    1. Product Name: 4-(3-oxo-1-phenyl-3-thiophen-2-yl-propyl)-3,4-dihydro-1H-benzo[b]azepine-2,5-dione
    2. Synonyms:
    3. CAS NO:1026866-29-4
    4. Molecular Formula:
    5. Molecular Weight: 389.475
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1026866-29-4.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: 4-(3-oxo-1-phenyl-3-thiophen-2-yl-propyl)-3,4-dihydro-1H-benzo[b]azepine-2,5-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(3-oxo-1-phenyl-3-thiophen-2-yl-propyl)-3,4-dihydro-1H-benzo[b]azepine-2,5-dione(1026866-29-4)
    11. EPA Substance Registry System: 4-(3-oxo-1-phenyl-3-thiophen-2-yl-propyl)-3,4-dihydro-1H-benzo[b]azepine-2,5-dione(1026866-29-4)

  • 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: 1026866-29-4(Hazardous Substances Data)

1026866-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026866-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,8,6 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1026866-29:
(9*1)+(8*0)+(7*2)+(6*6)+(5*8)+(4*6)+(3*6)+(2*2)+(1*9)=154
154 % 10 = 4
So 1026866-29-4 is a valid CAS Registry Number.

1026866-29-4Relevant articles and documents

Antitumor pyrido[3,2-d][1]benzazepines: Synthesis and in vitro activity of thiophene analogs

Link,Zaharevitz,Kunick, Conrad

, p. 163 - 166 (2007/10/03)

The bioisosteric replacement of benzene elements in the antitumor lead structures 2 and 3 led to the thienyl substituted 5H-pyrido[3,2- d][1]benzazepin-6(7H)-ones 8a and 8b, the analogous thiolactams 4a and 4b, and the 4H-pyrido[2,3-d]thieno[3,2-b]azepine

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