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C52H44N11O6P3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379539-10-2 Structure
  • Basic information

    1. Product Name: C52H44N11O6P3
    2. Synonyms:
    3. CAS NO:1379539-10-2
    4. Molecular Formula:
    5. Molecular Weight: 1011.91
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379539-10-2.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: C52H44N11O6P3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C52H44N11O6P3(1379539-10-2)
    11. EPA Substance Registry System: C52H44N11O6P3(1379539-10-2)
  • 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: 1379539-10-2(Hazardous Substances Data)

1379539-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379539-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,5,3 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1379539-10:
(9*1)+(8*3)+(7*7)+(6*9)+(5*5)+(4*3)+(3*9)+(2*1)+(1*0)=202
202 % 10 = 2
So 1379539-10-2 is a valid CAS Registry Number.

1379539-10-2Downstream Products

1379539-10-2Relevant articles and documents

Synthesis and characterization of side group-modified tetradentate cyclotriphosphazene derivatives

Yang,Zou,Li,Yang,Ye,Zhao

, p. 722 - 727 (2012/07/27)

A series of novel side group-modified cyclotriphosphazene derivatives were synthesized by the reaction of hexachlorocyclotriphosphazene [N 3P3Cl6] with 2,2-diphenol and the potassium salt of 4-hydroxybenzaldehyde, and subsequent reduction of aldehyde groups to alcohol groups by the use of sodium borohydride. The bromination reaction was carried out with PBr3 to give N3P3(O 2C12H8) (p-BrCH2-C6H 4-O-)4. This compound was employed in reactions with macrocyclic polyamides, imidazole, or morpholine to produce title compounds. The target compounds were characterized by 1H NMR, 31P NMR, 13C NMR, and electrospray ionization mass spectrometry. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. Copyright

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