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CAS

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1383969-90-1

(2E,7E)-bis(2,5-dimethoxybenzylidene)cycloheptanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1383969-90-1 Structure

  • Basic information

    1. Product Name: (2E,7E)-bis(2,5-dimethoxybenzylidene)cycloheptanone
    2. Synonyms: (2E,7E)-bis(2,5-dimethoxybenzylidene)cycloheptanone
    3. CAS NO:1383969-90-1
    4. Molecular Formula:
    5. Molecular Weight: 408.494
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1383969-90-1.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: (2E,7E)-bis(2,5-dimethoxybenzylidene)cycloheptanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2E,7E)-bis(2,5-dimethoxybenzylidene)cycloheptanone(1383969-90-1)
    11. EPA Substance Registry System: (2E,7E)-bis(2,5-dimethoxybenzylidene)cycloheptanone(1383969-90-1)

  • 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: 1383969-90-1(Hazardous Substances Data)

1383969-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383969-90-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,9,6 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1383969-90:
(9*1)+(8*3)+(7*8)+(6*3)+(5*9)+(4*6)+(3*9)+(2*9)+(1*0)=221
221 % 10 = 1
So 1383969-90-1 is a valid CAS Registry Number.

1383969-90-1Downstream Products

1383969-90-1Relevant articles and documents

Synthesis and biological evaluation of new curcumin derivatives as antioxidant and antitumor agents

Bayomi, Said M.,El-Kashef, Hassan A.,El-Ashmawy, Mahmoud B.,Nasr, Magda N. A.,El-Sherbeny, Magda A.,Badria, Farid A.,Abou-Zeid, Laila A.,Ghaly, Mariam A.,Abdel-Aziz, Naglaa I.

, p. 1147 - 1162 (2013)

Twenty-four new compounds were prepared, taking curcumin as a lead, in order to explore their antioxidant and antitumor properties. The capacities of these derivatives to scavenge the 2,2′-azinobis(3-ethylbenzothiazoline-6- sulfonic acid) radical cation (ABTS.+), and to protect human red blood cells (RBCs) from oxidative haemolysis were investigated. In addition, the percentage viability of different cell lines (Hep G2, WI38, VERO and MCF-7) was tested. The result of the antitumor testing was generally in accordance with those of the antioxidant assays. Compounds which bear o-methoxy substitution to the 4-hydroxy function in the phenyl ring (7g, 5g and 3g) exhibited significantly higher ABTS.+-scavenging, antihaemolysis, and antitumor activities than other derivatives. In addition, molecular modelling studies were carried out for biologically active and inactive compounds, to study the structure-activity relationship, with the aim to elucidate which portions of the molecules are critical for the antioxidant and antitumor activity.

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