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105972-87-0

di(2-chlorophenyl) chloromethylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105972-87-0 Structure

  • Basic information

    1. Product Name: di(2-chlorophenyl) chloromethylphosphonate
    2. Synonyms:
    3. CAS NO:105972-87-0
    4. Molecular Formula:
    5. Molecular Weight: 351.553
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105972-87-0.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: di(2-chlorophenyl) chloromethylphosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: di(2-chlorophenyl) chloromethylphosphonate(105972-87-0)
    11. EPA Substance Registry System: di(2-chlorophenyl) chloromethylphosphonate(105972-87-0)

  • 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: 105972-87-0(Hazardous Substances Data)

105972-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105972-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,7 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105972-87:
(8*1)+(7*0)+(6*5)+(5*9)+(4*7)+(3*2)+(2*8)+(1*7)=140
140 % 10 = 0
So 105972-87-0 is a valid CAS Registry Number.

105972-87-0Relevant articles and documents

Synthesis and preliminary biochemical studies with 5'-deoxy-5'-methylidyne phosphonate linked thymidine oligonucleotides

Zhao, Zhengyun,Caruthers, Marvin H.

, p. 6239 - 6242 (2007/10/03)

Thymidine deoxyoligonucleotides having a 5'-deoxy-5'-methylidyne phosphonate internucleotide linkage were synthesized. Relative to natural DNA, these oligomers were nuclease resistant and formed duplexes with reduced stability.

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