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76185-26-7

(μ-Se2)(carbonyl)6diiron is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76185-26-7 Structure

  • Basic information

    1. Product Name: (μ-Se2)(carbonyl)6diiron
    2. Synonyms: (μ-Se2)(carbonyl)6diiron
    3. CAS NO:76185-26-7
    4. Molecular Formula:
    5. Molecular Weight: 437.676
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76185-26-7.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: (μ-Se2)(carbonyl)6diiron(CAS DataBase Reference)
    10. NIST Chemistry Reference: (μ-Se2)(carbonyl)6diiron(76185-26-7)
    11. EPA Substance Registry System: (μ-Se2)(carbonyl)6diiron(76185-26-7)

  • 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: 76185-26-7(Hazardous Substances Data)

76185-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76185-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,8 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76185-26:
(7*7)+(6*6)+(5*1)+(4*8)+(3*5)+(2*2)+(1*6)=147
147 % 10 = 7
So 76185-26-7 is a valid CAS Registry Number.

76185-26-7Relevant articles and documents

Asymmetric cleavage of biscycloalka-1,4-diselena-2,5-cyclohexadienes and 1,4-diselenafulvenes by iron nonacarbonyl including the isolation of intermediate metallapropellanes

Mayr, Armin J.,Lien, Hsun-Shan,Pannell, Keith H.,Parkanyi, Laszlo

, p. 1580 - 1585 (2008/10/08)

Reactions of Fe2(CO)9 with various biscycloalka-1,4-diselena-2,5-cyclohexadienes lead to a variety of products: (diselenato)diiron hexacarbonyls, ferracyclohexadienones, ferracyclopentadienes, cycloalkenobenzenes, and unique diiron diselenametallapropellanes. These latter complexes are intermediates in the fragmentation of the starting heterocycles to the other observed products. The nature of the exact product distribution from the reactions depends upon the ring size of the starting heterocycle. An X-ray crystallographic analysis of a metallapropellane is reported. Reactions of 1,4-diselenafulvenes are also reported, leading to a related asymmetric cleavage to form (diselenato)diiron hexacarbonyl complexes but with no isolable or observable products from the remaining organic fragment. With a styryl-substituted diselenafulvene, an unusual triiron nonacarbonyl complex is isolated.

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