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1308881-19-7

4-propyl-N-(4-(5-(4-propylbenzamido)benzo[d]oxazol-2-yl)phenyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1308881-19-7 Structure

  • Basic information

    1. Product Name: 4-propyl-N-(4-(5-(4-propylbenzamido)benzo[d]oxazol-2-yl)phenyl)benzamide
    2. Synonyms:
    3. CAS NO:1308881-19-7
    4. Molecular Formula:
    5. Molecular Weight: 517.627
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1308881-19-7.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-propyl-N-(4-(5-(4-propylbenzamido)benzo[d]oxazol-2-yl)phenyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-propyl-N-(4-(5-(4-propylbenzamido)benzo[d]oxazol-2-yl)phenyl)benzamide(1308881-19-7)
    11. EPA Substance Registry System: 4-propyl-N-(4-(5-(4-propylbenzamido)benzo[d]oxazol-2-yl)phenyl)benzamide(1308881-19-7)

  • 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: 1308881-19-7(Hazardous Substances Data)

1308881-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1308881-19-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,8,8,8 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1308881-19:
(9*1)+(8*3)+(7*0)+(6*8)+(5*8)+(4*8)+(3*1)+(2*1)+(1*9)=167
167 % 10 = 7
So 1308881-19-7 is a valid CAS Registry Number.

1308881-19-7Downstream Products

1308881-19-7Relevant articles and documents

Synthesis and Preliminary Biologic Evaluation of 5-Substituted-2-(4-substituted phenyl)-1,3-Benzoxazoles as A Novel Class of Influenza Virus A Inhibitors

Li, Zhenyu,Zhan, Peng,Naesens, Lieve,Vanderlinden, Evelien,Liu, Ailin,Du, Guanhua,De Clercq, Erik,Liu, Xinyong

, p. 1018 - 1024 (2012/07/30)

The diversity-oriented chemistry synthesis together with the random screening approach has permitted the discovery and optimization of novel antiviral lead compounds. In this paper, a series of novel 5-substituted-2-(4-substituted phenyl)-1,3-benzoxazoles was synthesized and evaluated for their in vitro anti-influenza A virus and anti-influenza B virus activity. The activity was monitored by the MTS assay in the Madin-Darby canine kidney cells. Compound 7h showed excellent inhibitory activity and selective index against A/H3N2 (EC50=37.03μm, SI>5), which were all higher than that of the reference drug oseltamivir (EC50>59.00μm, SI>1). However, no compound displays inhibitory activity against influenza B virus.

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