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N-(2,4,6-tri-tert-butylphenyl)imino(pentafluorophenyl)phosphane iron tetracarbonyl adduct is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1309767-04-1 Structure
  • Basic information

    1. Product Name: N-(2,4,6-tri-tert-butylphenyl)imino(pentafluorophenyl)phosphane iron tetracarbonyl adduct
    2. Synonyms: N-(2,4,6-tri-tert-butylphenyl)imino(pentafluorophenyl)phosphane iron tetracarbonyl adduct
    3. CAS NO:1309767-04-1
    4. Molecular Formula:
    5. Molecular Weight: 625.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1309767-04-1.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: N-(2,4,6-tri-tert-butylphenyl)imino(pentafluorophenyl)phosphane iron tetracarbonyl adduct(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2,4,6-tri-tert-butylphenyl)imino(pentafluorophenyl)phosphane iron tetracarbonyl adduct(1309767-04-1)
    11. EPA Substance Registry System: N-(2,4,6-tri-tert-butylphenyl)imino(pentafluorophenyl)phosphane iron tetracarbonyl adduct(1309767-04-1)
  • 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: 1309767-04-1(Hazardous Substances Data)

1309767-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1309767-04-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,7,6 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1309767-04:
(9*1)+(8*3)+(7*0)+(6*9)+(5*7)+(4*6)+(3*7)+(2*0)+(1*4)=171
171 % 10 = 1
So 1309767-04-1 is a valid CAS Registry Number.

1309767-04-1Downstream Products

1309767-04-1Relevant articles and documents

Synthesis of blue imino(pentafluorophenyl)phosphane

Kuprat, Marcus,Lehmann, Mathias,Schulz, Axel,Villinger, Alexander

, p. 5784 - 5792 (2011)

The reaction of AgC6F5 with monomeric iminophosphanes of Mes*-N=P-X (X = Cl, I) in CH2Cl2 at ambient temperature gives imino(pentafluorophenyl)phosphane, Mes*N=P(C 6F5) (1), in almost quantitative yield (96%), which could be isolated as a highly viscous blue oil. The same reaction with LiC 6F5 results in the formation of imino(amino)phosphane (C6F5)2P-N(Mes*)-P=NMes* (2) (yield 93%). In the second series of experiments the analogous reaction of MC 6F5 (M = Ag, Li) with dimeric [Cl-P(μ-N-Dipp)] 2 was studied, leading to the formation of [R-P(μ-N-Dipp)] 2 (R = C6F5) (3) for M = Ag, while only decomposition products such as P(C6F5)3 were observed in the reaction with the Li salt. Highly labile Mes*-N=P-C 6F5 (1) decomposes at ambient temperatures, forming among other products the diphosphane (C6F5)2P- P(C6F5)2 (4). Reaction of 1 with Fe 2(CO)9 yields the iron carbonyl complexes Mes*-N=P(C6F5)?Fe(CO)4 (5) and [Mes*-N=P(C6F5)]2?Fe(CO) 3 (6). The structure, bonding, and potential energy surface are discussed on the basis of B3LYP/6-31G(d,p) computations. According to time-dependent B3LYP calculations, the blue color of 1 arises from an n → π* electronic transition.

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