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acetic acid (E)-2-acetoxy-4-(3-oxo-7-phenyl-hept-1-enyl)phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1443545-69-4 Structure
  • Basic information

    1. Product Name: acetic acid (E)-2-acetoxy-4-(3-oxo-7-phenyl-hept-1-enyl)phenyl ester
    2. Synonyms: acetic acid (E)-2-acetoxy-4-(3-oxo-7-phenyl-hept-1-enyl)phenyl ester
    3. CAS NO:1443545-69-4
    4. Molecular Formula:
    5. Molecular Weight: 380.441
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1443545-69-4.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: acetic acid (E)-2-acetoxy-4-(3-oxo-7-phenyl-hept-1-enyl)phenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: acetic acid (E)-2-acetoxy-4-(3-oxo-7-phenyl-hept-1-enyl)phenyl ester(1443545-69-4)
    11. EPA Substance Registry System: acetic acid (E)-2-acetoxy-4-(3-oxo-7-phenyl-hept-1-enyl)phenyl ester(1443545-69-4)
  • 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: 1443545-69-4(Hazardous Substances Data)

1443545-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1443545-69-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,5,4 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1443545-69:
(9*1)+(8*4)+(7*4)+(6*3)+(5*5)+(4*4)+(3*5)+(2*6)+(1*9)=164
164 % 10 = 4
So 1443545-69-4 is a valid CAS Registry Number.

1443545-69-4Downstream Products

1443545-69-4Relevant articles and documents

Synthesis and neuroprotective effect of E-3,4-dihydroxy styryl aralkyl ketones derivatives against oxidative stress and inflammation

Ning, Xianling,Guo, Ying,Ma, Xiaoyan,Zhu, Renzong,Tian, Chao,Wang, Xiaowei,Ma, Zhizhong,Zhang, Zhili,Liu, Junyi

, p. 3700 - 3703 (2013/07/25)

E-3,4-Dihydroxy styryl aralkyl ketones as well as their 3,4-diacetylated derivatives as the analogues of neuroprotective agent CAPE were designed and synthesized for improving stability and lipid solubility. The neuroprotective activities of target compounds 10a-g and 11a-g were tested by three models in vitro, including 1,1-diphenyl-2-picrylhydrazyl radical scavenging capacity, neuronal protecting effect against damage induced by H2O2 in PC12 cells and nitric oxide suppression effect in BV2 microglial cells. The results demonstrated that compounds 10f and 11f exhibited the most potent neuroprotective effect against oxidative stress and inflammation, which is higher than that of the lead compound CAPE.

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