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CAS

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1326315-89-2

[(CuO(N(CH2CH2C5H4N)2(CH2C6H4OH)))2](2+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1326315-89-2 Structure

  • Basic information

    1. Product Name: [(CuO(N(CH2CH2C5H4N)2(CH2C6H4OH)))2](2+)
    2. Synonyms:
    3. CAS NO:1326315-89-2
    4. Molecular Formula:
    5. Molecular Weight: 825.957
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1326315-89-2.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: [(CuO(N(CH2CH2C5H4N)2(CH2C6H4OH)))2](2+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: [(CuO(N(CH2CH2C5H4N)2(CH2C6H4OH)))2](2+)(1326315-89-2)
    11. EPA Substance Registry System: [(CuO(N(CH2CH2C5H4N)2(CH2C6H4OH)))2](2+)(1326315-89-2)

  • 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: 1326315-89-2(Hazardous Substances Data)

1326315-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1326315-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,6,3,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1326315-89:
(9*1)+(8*3)+(7*2)+(6*6)+(5*3)+(4*1)+(3*5)+(2*8)+(1*9)=142
142 % 10 = 2
So 1326315-89-2 is a valid CAS Registry Number.

1326315-89-2Upstream product

1326315-89-2Downstream Products

1326315-89-2Relevant articles and documents

Benzylic ligand hydroxylation starting from a dicopper μ- I·2:I·2 peroxo intermediate: Dramatic acceleration of the reaction by hydrogen-atom donors

Rolff, Malte,Hamann, Jessica Nadine,Tuczek, Felix

, p. 6924 - 6927 (2011)

Radicals in directed pathways: The μ-I·2: I·2 peroxo CuII2 intermediate 1 shows a much faster benzylic ligand hydroxylation than systems without phenol. This novel reactivity can be further accelerated by addition of external H-atom donors such as TEMPO-H. The results imply initial H-atom transfer leading to the formation of phenoxyl radicals. A highly reactive copper oxyl intermediate is then formed, which inserts oxygen into the benzylic C-H bond. Copyright

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