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CAS

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1313751-08-4

4,5-bis(4-nitrophenyl)-2H-1,2,3-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1313751-08-4 Structure

  • Basic information

    1. Product Name: 4,5-bis(4-nitrophenyl)-2H-1,2,3-triazole
    2. Synonyms: 4,5-bis(4-nitrophenyl)-2H-1,2,3-triazole
    3. CAS NO:1313751-08-4
    4. Molecular Formula:
    5. Molecular Weight: 311.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1313751-08-4.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: 4,5-bis(4-nitrophenyl)-2H-1,2,3-triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,5-bis(4-nitrophenyl)-2H-1,2,3-triazole(1313751-08-4)
    11. EPA Substance Registry System: 4,5-bis(4-nitrophenyl)-2H-1,2,3-triazole(1313751-08-4)

  • 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: 1313751-08-4(Hazardous Substances Data)

1313751-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1313751-08-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,7,5 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1313751-08:
(9*1)+(8*3)+(7*1)+(6*3)+(5*7)+(4*5)+(3*1)+(2*0)+(1*8)=124
124 % 10 = 4
So 1313751-08-4 is a valid CAS Registry Number.

1313751-08-4Relevant articles and documents

Transition Metal, Azide, and Oxidant-Free Homo- and Heterocoupling of Ambiphilic Tosylhydrazones to the Regioselective Triazoles and Pyrazoles

Panda, Subhankar,Maity, Pradip,Manna, Debasis

supporting information, p. 1534 - 1537 (2017/04/13)

With N-tosylhydrazone as an ambiphilic reagent, an unprecedented cyclization reaction of two identical or different tosylhydrazones has been developed to access various 4,5-disubstituted-2H-triazoles under transition metal, azide, and oxidant-free conditi

HCV NS5A replication complex inhibitors. Part 3

Lopez, Omar D.,Nguyen, Van N.,St. Laurent, Denis R.,Belema, Makonen,Serrano-Wu, Michael H.,Goodrich, Jason T.,Yang, Fukang,Qiu, Yuping,Ripka, Amy S.,Nower, Peter T.,Valera, Lourdes,Liu, Mengping,O'Boyle II, Donald R.,Sun, Jin-Hua,Fridell, Robert A.,Lemm, Julie A.,Gao, Min,Good, Andrew C.,Meanwell, Nicholas A.,Snyder, Lawrence B.

, p. 779 - 784 (2013/02/25)

In a recent disclosure,1 we described the discovery of dimeric, prolinamide-based NS5A replication complex inhibitors exhibiting excellent potency towards an HCV genotype 1b replicon. That disclosure dealt with the SAR exploration of the peripheral region of our lead chemotype, and herein is described the SAR uncovered from a complementary effort that focused on the central core region. From this effort, the contribution of the core region to the overall topology of the pharmacophore, primarily vector orientation and planarity, was determined, with a set of analogs exhibiting 50 in a genotype 1b replicon assay.

HEPATITIS C VIRUS INHIBITORS

-

Page/Page column 271-272, (2011/07/30)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such compounds, and methods for inhibiting the function of the NS5A protein

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