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  • 1243300-87-9 Structure
  • Basic information

    1. Product Name: C32H21AsF12O3
    2. Synonyms: C32H21AsF12O3
    3. CAS NO:1243300-87-9
    4. Molecular Formula:
    5. Molecular Weight: 756.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1243300-87-9.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: C32H21AsF12O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C32H21AsF12O3(1243300-87-9)
    11. EPA Substance Registry System: C32H21AsF12O3(1243300-87-9)
  • 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: 1243300-87-9(Hazardous Substances Data)

1243300-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1243300-87-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,3,0 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1243300-87:
(9*1)+(8*2)+(7*4)+(6*3)+(5*3)+(4*0)+(3*0)+(2*8)+(1*7)=109
109 % 10 = 9
So 1243300-87-9 is a valid CAS Registry Number.

1243300-87-9Downstream Products

1243300-87-9Relevant articles and documents

Formation of epoxides from pentacoordinated organoarsenic compounds with a β-hydroxyethyl group

Jiang, Xin-Dong,Matsukawa, Shiro,Fukuzaki, Yuta,Yamamoto, Yohsuke

experimental part, p. 1623 - 1629 (2010/10/04)

A series of pentacoordinated organoarsenic compounds (arsoranes) bearing a β-hydroxyethyl group (4a, 6a and 6b) was synthesized. The crystal structures were determined by single crystal X-ray analysis. Treatment of these arsoranes with KH almost quantitatively gave the corresponding epoxide. The reaction of 4a having an unsubstituted β-hydroxyethyl group with KH was monitored by 1H and 19F NMR in CD3CN, suggesting that a hexacoordinate arsenic anion was formed as the intermediate. However, a further stereochemical study of the epoxide formation suggested that the reaction proceeded in the SN2 manner and not in the ligand coupling reaction (LCR) of the intermediate hexacoordinate arsenic anion.

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