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C16H13ClF4O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1426242-46-7 Structure
  • Basic information

    1. Product Name: C16H13ClF4O3
    2. Synonyms:
    3. CAS NO:1426242-46-7
    4. Molecular Formula:
    5. Molecular Weight: 364.724
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1426242-46-7.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: C16H13ClF4O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H13ClF4O3(1426242-46-7)
    11. EPA Substance Registry System: C16H13ClF4O3(1426242-46-7)
  • 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: 1426242-46-7(Hazardous Substances Data)

1426242-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426242-46-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,2,4 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1426242-46:
(9*1)+(8*4)+(7*2)+(6*6)+(5*2)+(4*4)+(3*2)+(2*4)+(1*6)=137
137 % 10 = 7
So 1426242-46-7 is a valid CAS Registry Number.

1426242-46-7Downstream Products

1426242-46-7Relevant articles and documents

Accelerating Ni(ii) precatalyst initiation using reactive ligands and its impact on chain-growth polymerizations

Lee, Se Ryeon,Bloom, Jacob W. G.,Wheeler, Steven E.,McNeil, Anne J.

, p. 4218 - 4222 (2013)

Nickel(ii) complexes with varying reactive ligands, which were designed to selectively accelerate the initiation rate without influencing the propagation rate in the chain-growth polymerization of π-conjugated monomers, were investigated. Precatalysts with electronically varied reacting groups led to faster initiation rates and narrower molecular weight distributions. Computational studies revealed that the reductive elimination rates are largely modulated by the ability of the two reacting arenes to stabilize the increasing electron density on the catalyst during reductive elimination. Overall, these studies provide insight into a key mechanistic step of cross-coupling reactions (reductive elimination) and highlight the importance of initiation in controlled chain-growth polymerizations.

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