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1347740-14-0

C16H28NO3P is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1347740-14-0 Structure

  • Basic information

    1. Product Name: C16H28NO3P
    2. Synonyms: C16H28NO3P
    3. CAS NO:1347740-14-0
    4. Molecular Formula:
    5. Molecular Weight: 313.377
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1347740-14-0.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: C16H28NO3P(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H28NO3P(1347740-14-0)
    11. EPA Substance Registry System: C16H28NO3P(1347740-14-0)

  • 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: 1347740-14-0(Hazardous Substances Data)

1347740-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1347740-14-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,7,7,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1347740-14:
(9*1)+(8*3)+(7*4)+(6*7)+(5*7)+(4*4)+(3*0)+(2*1)+(1*4)=160
160 % 10 = 0
So 1347740-14-0 is a valid CAS Registry Number.

1347740-14-0Relevant articles and documents

Synthesis and biological evaluation of novel phosphonates derivatives of as potential antitumor agents

Jin, Chuanfei,Liang, Yong-Ju,He, Hongwu,Fu, Liwu

, p. 2096 - 2103 (2011/12/01)

A series of dialkyl [2-(4,6-dimethoxypyrimidin-2-yloxy)benzamido](aryl) methylphosphonates derivatives were designed and synthesized. All the new compounds were identified by elemental analysis, IR, 1H NMR, 31P NMR, and MS. Their antitumor activity against KB and CNE1 cells was examined. Some of the compounds showed potential antitumor activity, which provided some hints for further study of structure modification. In particular, the compounds 6i and 6j displayed more potent cytotoxic activities against KB in comparison with 5-FU. Copyright Taylor & Francis Group, LLC.

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