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180139-02-0

C13H11Cl4NP2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 180139-02-0 Structure

  • Basic information

    1. Product Name: C13H11Cl4NP2
    2. Synonyms: C13H11Cl4NP2
    3. CAS NO:180139-02-0
    4. Molecular Formula:
    5. Molecular Weight: 384.997
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 180139-02-0.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: C13H11Cl4NP2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H11Cl4NP2(180139-02-0)
    11. EPA Substance Registry System: C13H11Cl4NP2(180139-02-0)

  • 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: 180139-02-0(Hazardous Substances Data)

180139-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180139-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,1,3 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 180139-02:
(8*1)+(7*8)+(6*0)+(5*1)+(4*3)+(3*9)+(2*0)+(1*2)=110
110 % 10 = 0
So 180139-02-0 is a valid CAS Registry Number.

180139-02-0Upstream product

180139-02-0Downstream Products

180139-02-0Relevant articles and documents

Reaction of N-alkylpyredinium salts with phosphorus trichloride

Bansal, Raj K.,Gupta, Neelima,Gupta, Rakhi,Pandey, Garima,Agarwal, Mamta

, p. 121 - 130 (2007/10/03)

1-Alkylpyridinium bromides 1 having activated N-methylene group react with phosphorus trichloride to give N-(dichlorophosphinomethylene)pyridinium ylides 2. The site of the reaction in 1,2-dialkylpyridinium halides 3 under these conditions is determined by the relative activation of 1- and 2-methylene groups; in the absence of sufficient activation of N-methylene group, reaction occurs at the 2-methylene group to give dichlorophosphinylated anhydrobases 5 and 11. 1,4-Dialkylpyridinium bromide 13 behaves analogously to give the corresponding dichlorophosphinylated anhydrobase 14.

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