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CAS

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84322-80-5

1-Diethoxyphosphonyl-3-methyl-3-phenyltriazen is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84322-80-5 Structure

  • Basic information

    1. Product Name: 1-Diethoxyphosphonyl-3-methyl-3-phenyltriazen
    2. Synonyms: 1-Diethoxyphosphonyl-3-methyl-3-phenyltriazen
    3. CAS NO:84322-80-5
    4. Molecular Formula:
    5. Molecular Weight: 271.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84322-80-5.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: 1-Diethoxyphosphonyl-3-methyl-3-phenyltriazen(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Diethoxyphosphonyl-3-methyl-3-phenyltriazen(84322-80-5)
    11. EPA Substance Registry System: 1-Diethoxyphosphonyl-3-methyl-3-phenyltriazen(84322-80-5)

  • 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: 84322-80-5(Hazardous Substances Data)

84322-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84322-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,2 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84322-80:
(7*8)+(6*4)+(5*3)+(4*2)+(3*2)+(2*8)+(1*0)=125
125 % 10 = 5
So 84322-80-5 is a valid CAS Registry Number.

84322-80-5Relevant articles and documents

Phosphonyl- and Phosphinyl-triazenes. Electrophilic Substitution Reactions with Benzene

Kreher, Richard,Halpaap, Reinhard

, p. 1178 - 1183 (2007/10/02)

The reaction of phosphonyltriazenes with benzene in the presence of aluminiumchloride is involved with the elimination of nitrogen and followed by electrophilic substitution of benzene.The arylation reaction obviously proceeds via the intermediate formation of arene diazonium ions.Phosphinyltriazenes display the same chemical behaviour. - Key words: Phosphonyl- and Phosphinyl-triazenes, N2-Elimination, Electrophilic Substitution Reactions with Benzene

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