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848-54-4

Tris(4-fluorophenyl)aluminum is an organoaluminum compound with the chemical formula C18H12AlF3. It is a colorless, crystalline solid that is highly sensitive to air and moisture. tris(4-fluorophenyl)aluminum is formed by the coordination of three 4-fluorophenyl ligands to an aluminum center. Tris(4-fluorophenyl)aluminum is used as a catalyst in various organic reactions, particularly in the polymerization of olefins and the synthesis of certain organic compounds. Due to its reactivity, it is typically handled under an inert atmosphere or in a vacuum to prevent unwanted side reactions.

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  • 848-54-4 Structure

  • Basic information

    1. Product Name: tris(4-fluorophenyl)aluminum
    2. Synonyms: tris(4-fluorophenyl)aluminum
    3. CAS NO:848-54-4
    4. Molecular Formula:
    5. Molecular Weight: 312.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 848-54-4.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: tris(4-fluorophenyl)aluminum(CAS DataBase Reference)
    10. NIST Chemistry Reference: tris(4-fluorophenyl)aluminum(848-54-4)
    11. EPA Substance Registry System: tris(4-fluorophenyl)aluminum(848-54-4)

  • 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: 848-54-4(Hazardous Substances Data)

848-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848-54-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 848-54:
(5*8)+(4*4)+(3*8)+(2*5)+(1*4)=94
94 % 10 = 4
So 848-54-4 is a valid CAS Registry Number.

848-54-4Relevant articles and documents

The inexpensive additive N-methylmorpholine effectively decreases the equivalents of nucleophiles in the catalytic highly enantioselective arylation of aryl aldehydes

Wang, Pei,Liu, Yue,Zhang, Ya-Lun,Da, Chao-Shan

supporting information, p. 443 - 450 (2017/07/25)

Highly enantioselective arylation of aryl aldehydes catalyzed by (S)-H8-BINOL-Ti(Oi-Pr)2 complex in the presence of N-methylmorpholine (NMM) as an effective and inexpensive additive is described for the first time. We found high enan

Sequential [3,3]-Sigmatropic Rearrangement/Nucleophilic Arylation of N -(Benzoyloxy)enamides towards the Preparation of Cyclic β-Aryl-β-amino Alcohols

Sato, Shohei,Takeda, Norihiko,Ueda, Masafumi,Miyata, Okiko

, p. 882 - 892 (2016/03/15)

A new method has been developed for the efficient synthesis of cyclic β-aryl-β-amino alcohol derivatives bearing a tetrasubstituted carbon center via the [3,3]-sigmatropic rearrangement of N-(benzoyl oxy)enamides followed by nucleophilic arylation reactio

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