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CAS

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133910-04-0

3-(4'-methylbiphenyl-2-yl)-5-(trifluoromethyl)-N-(triphenylmethyl)-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133910-04-0 Structure

  • Basic information

    1. Product Name: 3-(4'-methylbiphenyl-2-yl)-5-(trifluoromethyl)-N-(triphenylmethyl)-1,2,4-triazole
    2. Synonyms: 3-(4'-methylbiphenyl-2-yl)-5-(trifluoromethyl)-N-(triphenylmethyl)-1,2,4-triazole
    3. CAS NO:133910-04-0
    4. Molecular Formula:
    5. Molecular Weight: 545.607
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133910-04-0.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: 3-(4'-methylbiphenyl-2-yl)-5-(trifluoromethyl)-N-(triphenylmethyl)-1,2,4-triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4'-methylbiphenyl-2-yl)-5-(trifluoromethyl)-N-(triphenylmethyl)-1,2,4-triazole(133910-04-0)
    11. EPA Substance Registry System: 3-(4'-methylbiphenyl-2-yl)-5-(trifluoromethyl)-N-(triphenylmethyl)-1,2,4-triazole(133910-04-0)

  • 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: 133910-04-0(Hazardous Substances Data)

133910-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133910-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 133910-04:
(8*1)+(7*3)+(6*3)+(5*9)+(4*1)+(3*0)+(2*0)+(1*4)=100
100 % 10 = 0
So 133910-04-0 is a valid CAS Registry Number.

133910-04-0Relevant articles and documents

Nonpeptide Angiotensin II Receptor Antagonists: The Discovery of a Series of N-(Biphenylylmethyl)imidazoles as Potent, Orally Active Antihypertensives

Carini, David J.,Duncia, John V.,Aldrich, Paul E.,Chiu, Andrew T.,Johnson, Alexander L.,et al.

, p. 2525 - 2547 (1991)

A new series of nonpeptide angiotensin II (AII) receptor antagonists has been prepared.These N-(biphenylylmethyl)imidazoles, e.g. 2-butyl-1--4-chloro-5-(hydroxymethyl)imidazole, differ from the previously reported N-(benzamidobenzyl)imidazoles and related compounds in that they produce a potent antihypertensive effect upon oral administration; the earlier series generally were active only when administered intravenously.It has been found that the acidic group at the 2'-position of the biphenyl is essential.Only ortho-substituted acids possess both high affinity for the AII receptor and good oral antihypertensive potency.The carboxylic acid group has been replaced with a variety of acidic isosteres, and the tetrazole ring has been found to be the most effective.The tetrazole derivative, DuP 753, is currently in development for the treatment of hypertension.

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