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1114899-83-0

(3,5-bis(trifluoromethyl)phenyl)(4-chlorophenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1114899-83-0 Structure

  • Basic information

    1. Product Name: (3,5-bis(trifluoromethyl)phenyl)(4-chlorophenyl)methanone
    2. Synonyms: (3,5-bis(trifluoromethyl)phenyl)(4-chlorophenyl)methanone
    3. CAS NO:1114899-83-0
    4. Molecular Formula:
    5. Molecular Weight: 352.663
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1114899-83-0.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: (3,5-bis(trifluoromethyl)phenyl)(4-chlorophenyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3,5-bis(trifluoromethyl)phenyl)(4-chlorophenyl)methanone(1114899-83-0)
    11. EPA Substance Registry System: (3,5-bis(trifluoromethyl)phenyl)(4-chlorophenyl)methanone(1114899-83-0)

  • 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: 1114899-83-0(Hazardous Substances Data)

1114899-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1114899-83-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,4,8,9 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1114899-83:
(9*1)+(8*1)+(7*1)+(6*4)+(5*8)+(4*9)+(3*9)+(2*8)+(1*3)=170
170 % 10 = 0
So 1114899-83-0 is a valid CAS Registry Number.

1114899-83-0Downstream Products

1114899-83-0Relevant articles and documents

Photo-nickel dual catalytic benzoylation of aryl bromides

Schirmer, Tobias Emanuel,Wimmer, Alexander,Weinzierl, Florian Wolfgang Clemens,K?nig, Burkhard

, p. 10796 - 10799 (2019)

The dual catalytic arylation of aromatic aldehydes by aryl bromides using UV-irradiation and a nickel catalyst is reported. The reaction product serves as a photocatalyst and a hydrogen atom transfer agent for this transformation.

Functionalizations of Mixtures of Regioisomeric Aryllithium Compounds by Selective Trapping with Dichlorozirconocene

Castell-Mic, Alicia,Herbert, Simon A.,Len, Thierry,Bein, Thomas,Knochel, Paul

supporting information, p. 401 - 404 (2016/01/25)

The reaction of mixtures of aryllithium regioisomers obtained either by directed lithiation or by Br/Li exchange with substoichiometric amounts of Cp2ZrCl2 proceeds with high regioselectivity. The least sterically hindered regioisome

A novel Br?nsted acid catalyst for Friedel-Crafts acylation

Posternak, Anna G.,Garlyauskayte, Romute Yu.,Yagupolskii, Lev M.

supporting information; body text, p. 446 - 447 (2009/05/27)

Bis(trifluoroalkylsulfonylimino)trifluoromethanesulfonic acid has demonstrated remarkable catalytic ability in the electrophilic acylation of aromatic substrates. Various perfluoroalkyl substituted aroyl chlorides are employed in Friedel-Crafts acylation typically using 1 mol % of catalyst. Crown Copyright

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