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CAS

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177574-06-0

5-(2,5-DIMETHYLPHENYL)-2H-TETRAAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 177574-06-0 Structure

  • Basic information

    1. Product Name: 5-(2,5-DIMETHYLPHENYL)-2H-TETRAAZOLE
    2. Synonyms: 5-(2,5-DIMETHYLPHENYL)-2H-TETRAAZOLE
    3. CAS NO:177574-06-0
    4. Molecular Formula: C9H10N4
    5. Molecular Weight: 174.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177574-06-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-(2,5-DIMETHYLPHENYL)-2H-TETRAAZOLE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(2,5-DIMETHYLPHENYL)-2H-TETRAAZOLE(177574-06-0)
    11. EPA Substance Registry System: 5-(2,5-DIMETHYLPHENYL)-2H-TETRAAZOLE(177574-06-0)

  • 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: 177574-06-0(Hazardous Substances Data)

177574-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177574-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,7 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 177574-06:
(8*1)+(7*7)+(6*7)+(5*5)+(4*7)+(3*4)+(2*0)+(1*6)=170
170 % 10 = 0
So 177574-06-0 is a valid CAS Registry Number.

177574-06-0Upstream product

177574-06-0Relevant articles and documents

(E)-1,2-bis(5-aryl-1,3,4-oxadiazol-2-yl)ethenes

Detert, Heiner,Schollmeier, Dieter

, p. 999 - 1004 (2007/10/03)

A series of (E)-1,2-bis(1,3,4-oxadiazol-2-yl)ethenes with a variety of aromatic substituents in the 5-positions of the heterocycles was prepared by acylation of the corresponding tetrazoles with fumaryl chloride and subsequent thermal ring transformation. The modified Huisgen reaction renders a new pathway to 3-(1,3,4-oxadiazol-2-yl)propenoic acids and subsequently to the title compounds with different substituents.

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