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1258606-08-4

(E)-1-(2,4-dichlorophenyl)-2-(3-chlorophenyl)ethene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1258606-08-4 Structure

  • Basic information

    1. Product Name: (E)-1-(2,4-dichlorophenyl)-2-(3-chlorophenyl)ethene
    2. Synonyms:
    3. CAS NO:1258606-08-4
    4. Molecular Formula:
    5. Molecular Weight: 283.584
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1258606-08-4.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: (E)-1-(2,4-dichlorophenyl)-2-(3-chlorophenyl)ethene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-(2,4-dichlorophenyl)-2-(3-chlorophenyl)ethene(1258606-08-4)
    11. EPA Substance Registry System: (E)-1-(2,4-dichlorophenyl)-2-(3-chlorophenyl)ethene(1258606-08-4)

  • 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: 1258606-08-4(Hazardous Substances Data)

1258606-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258606-08-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,6,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1258606-08:
(9*1)+(8*2)+(7*5)+(6*8)+(5*6)+(4*0)+(3*6)+(2*0)+(1*8)=164
164 % 10 = 4
So 1258606-08-4 is a valid CAS Registry Number.

1258606-08-4Downstream Products

1258606-08-4Relevant articles and documents

Synthesis and biological evaluation of some stilbene-based analogues

Karki, Subhas S.,Bhutle, Santosh R.,Pedgaonkar, Ganesh S.,Zubaidha,Shaikh, Rizwan M.,Rajput, Chitra G.,Shendarkar, Girish S.

, p. 1158 - 1163 (2012/05/05)

The phytoalexin 3,5,40-trihydroxy-trans-stilbene (resveratrol) has attracted considerable attention from biologists and chemists due to its diverse biological properties. Owing to the biological importance of this compound, we have synthesized new stilbene-based analogues by using substituted benzyl chlorides and substituted aldehydes in a two-step reaction and evaluated their in vitro antioxidant, antibacterial and antifungal potential. Most of the compounds displayed moderate to significant radical scavenging activity. (E)-1-(3,4-difluorophenyl)-2-(4-fluorophenyl) ethene (4c) showed nearer equipotent antibacterial activity against Staphylococcus aureus. (E)-1,2-bis (4-fluorophenyl)ethene (4a), (E)-1-(3-fluorophenyl)-2-(4-fluorophenyl)ethene (4b), (E)-1-(2,4-dichlorophenyl)-2-(3, 4-dichlorophenyl)ethene (4f), (E)-1-(2,4-dichlorophenyl)-2-(3-chlorophenyl)ethene (4g), (E)-1-(2,4- dichlorophenyl)-2-(4-fluorophenyl)ethene (4j) (E)-1-(4-fluorophenyl)-2-(3- chlorophenyl)ethene (4l) and (E)-1-(4-chlorophenyl)-2-(4-fluorophenyl)ethene (4n) inhibited the growth of Penicillium chrysogenum. Springer Science+Business Media, LLC 2010.

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