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C62H54Br2ClN10P3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 902140-67-4 Structure
  • Basic information

    1. Product Name: C62H54Br2ClN10P3
    2. Synonyms: C62H54Br2ClN10P3
    3. CAS NO:902140-67-4
    4. Molecular Formula:
    5. Molecular Weight: 1227.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 902140-67-4.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: C62H54Br2ClN10P3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C62H54Br2ClN10P3(902140-67-4)
    11. EPA Substance Registry System: C62H54Br2ClN10P3(902140-67-4)
  • 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: 902140-67-4(Hazardous Substances Data)

902140-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 902140-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,1,4 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 902140-67:
(8*9)+(7*0)+(6*2)+(5*1)+(4*4)+(3*0)+(2*6)+(1*7)=124
124 % 10 = 4
So 902140-67-4 is a valid CAS Registry Number.

902140-67-4Downstream Products

902140-67-4Relevant articles and documents

New macrobicyclic triphosphazides and triphosphazenes formed by self-assembly of tripodal triazides with triphosphanes

Alajarín, Mateo,López-Leonardo, Carmen,Berná, José

, p. 6190 - 6202 (2007/10/03)

The self-assembly of tris(3-azidobenzyl)amines with 1,1,1-tris[(diphenylphosphino)methyl]ethane via tripod-tripod coupling proceeds successfully to give chiral macrobicyclic triphosphazides. The heating of these macrobicyclic cages induces a remarkable stepwise triple extrusion of molecular nitrogen to afford tri-λ5-phosphazenes, which preserved the chiral, propeller-like topology of their precursors. The replacement of one benzylic arm by an ortho-phenethylic or propylenic one still allows the success of the self-assembly. However, the quaternization of the pivotal nitrogen atom of the triamine in the form of N-oxide prevented its coupling with the triphosphane.

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