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1,4-dicinnamoyl-1,4-diazepane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1164536-95-1 Structure
  • Basic information

    1. Product Name: 1,4-dicinnamoyl-1,4-diazepane
    2. Synonyms: 1,4-dicinnamoyl-1,4-diazepane
    3. CAS NO:1164536-95-1
    4. Molecular Formula: C23H24N2O2
    5. Molecular Weight: 360.44886
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1164536-95-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,4-dicinnamoyl-1,4-diazepane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-dicinnamoyl-1,4-diazepane(1164536-95-1)
    11. EPA Substance Registry System: 1,4-dicinnamoyl-1,4-diazepane(1164536-95-1)
  • 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: 1164536-95-1(Hazardous Substances Data)

1164536-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1164536-95-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,4,5,3 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1164536-95:
(9*1)+(8*1)+(7*6)+(6*4)+(5*5)+(4*3)+(3*6)+(2*9)+(1*5)=161
161 % 10 = 1
So 1164536-95-1 is a valid CAS Registry Number.

1164536-95-1Downstream Products

1164536-95-1Relevant articles and documents

Design, synthesis and antimycobacterial activity of cinnamide derivatives: A molecular hybridization approach

Kakwani, Manoj D.,Suryavanshi, Prashant,Ray, Muktikant,Rajan,Majee, Sharmila,Samad, Abdul,Devarajan, Padma,Degani, Mariam S.

, p. 1997 - 1999 (2011/05/02)

A series of cinnamide derivatives was designed as potential antimycobacterial agents using molecular hybridization approach. The diamine moiety, a key feature of ethambutol and its other analogs, and certain structural features of cerulenin and cinnamic a

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