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1401619-25-7

ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1401619-25-7 Structure

  • Basic information

    1. Product Name: ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate
    2. Synonyms: ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate
    3. CAS NO:1401619-25-7
    4. Molecular Formula:
    5. Molecular Weight: 327.81
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1401619-25-7.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: ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate(1401619-25-7)
    11. EPA Substance Registry System: ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate(1401619-25-7)

  • 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: 1401619-25-7(Hazardous Substances Data)

1401619-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401619-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,6,1 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1401619-25:
(9*1)+(8*4)+(7*0)+(6*1)+(5*6)+(4*1)+(3*9)+(2*2)+(1*5)=117
117 % 10 = 7
So 1401619-25-7 is a valid CAS Registry Number.

1401619-25-7Relevant articles and documents

Synthesis and biological activity of conformationally restricted indole-based inhibitors of neurotropic alphavirus replication: Generation of a three-dimensional pharmacophore

Barraza, Scott J.,Sindac, Janice A.,Dobry, Craig J.,Delekta, Philip C.,Lee, Pil H.,Miller, David J.,Larsen, Scott D.

, (2021)

We have previously reported the development of indole-based CNS-active antivirals for the treatment of neurotropic alphavirus infection, but further optimization is impeded by a lack of knowledge of the molecular target and binding site. Herein we describe the design, synthesis and evaluation of a series of conformationally restricted analogues with the dual objectives of improving potency/selectivity and identifying the most bioactive conformation. Although this campaign was only modestly successful at improving potency, the sharply defined SAR of the rigid analogs enabled the definition of a three-dimensional pharmacophore, which we believe will be of value in further analog design and virtual screening for alternative antiviral leads.

ARBOVIRUS INHIBITORS AND USES THEREOF

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Page/Page column 74, (2012/10/08)

The present invention relates to chemical compounds, methods for their discovery, and their therapeutic use. In particular, the present invention provides compounds as inhibitors of arboviruses.

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