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1104611-06-4

C22H38N4O16P4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1104611-06-4 Structure

  • Basic information

    1. Product Name: C22H38N4O16P4
    2. Synonyms:
    3. CAS NO:1104611-06-4
    4. Molecular Formula:
    5. Molecular Weight: 738.456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1104611-06-4.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: C22H38N4O16P4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H38N4O16P4(1104611-06-4)
    11. EPA Substance Registry System: C22H38N4O16P4(1104611-06-4)

  • 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: 1104611-06-4(Hazardous Substances Data)

1104611-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1104611-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,6,1 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1104611-06:
(9*1)+(8*1)+(7*0)+(6*4)+(5*6)+(4*1)+(3*1)+(2*0)+(1*6)=84
84 % 10 = 4
So 1104611-06-4 is a valid CAS Registry Number.

1104611-06-4Upstream product

1104611-06-4Downstream Products

1104611-06-4Relevant articles and documents

Bisphosphonate sequestering agents. Synthesis and preliminary evaluation for in vitro and in vivo uranium(VI) chelation

Sawicki, Marcin,Lecercle, Delphine,Grillon, Gerard,Le Gall, Beatrice,Serandour, Anne-Laure,Poncy, Jean-Luc,Bailly, Theodorine,Burgada, Ramon,Lecouvey, Marc,Challeix, Vincent,Leydier, Antoine,Pellet-Rostaing, Stephane,Ansoborlo, Eric,Taran, Frederic

, p. 2768 - 2777 (2008)

A library of bisphosphonate-based ligands was prepared using solution-phase parallel synthesis and tested for its uranium-binding properties. With the help of a screening method, based on a chromophoric complex displacement procedure, 23 dipodal and tripodal chelates bearing bisphosphonate chelating functions were found to display very high affinity for the uranyl ion and were selected for evaluation of their in vivo uranyl-removal efficacy. Among them, 11 ligands induced a huge modification of the uranyl biodistribution by deviating the metal from kidney and bones to liver. Among the other ligands, the most potent was the dipodal bisphosphonate 3C which reduced the retention of uranyl and increased its excretion by around 10% of the injected metal.

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