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Difluoro(4-chlorophenyl)-λ3-iodane is a chemical compound characterized by its unique structure and properties. It features a difluoro(4-chlorophenyl) group attached to an iodane moiety, which is a derivative of iodine. difluoro(4-chlorophenyl)-λ3-iodane is known for its potential applications in various chemical reactions and processes, particularly in the synthesis of pharmaceuticals and agrochemicals. Its chemical formula is C6H2ClF2I, indicating the presence of carbon, hydrogen, chlorine, fluorine, and iodine atoms. The compound's reactivity and stability are influenced by the electron-withdrawing nature of the fluorine atoms and the electron-donating effect of the chlorine atom, which can impact its behavior in different chemical environments.

350-45-8

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350-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350-45-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 350-45:
(5*3)+(4*5)+(3*0)+(2*4)+(1*5)=48
48 % 10 = 8
So 350-45-8 is a valid CAS Registry Number.

350-45-8Downstream Products

350-45-8Relevant academic research and scientific papers

Deconstructing the Catalytic, Vicinal Difluorination of Alkenes: HF-Free Synthesis and Structural Study of p-TolIF2

Sarie, Jér?me C.,Thiehoff, Christian,Mudd, Richard J.,Daniliuc, Constantin G.,Kehr, Gerald,Gilmour, Ryan

, p. 11792 - 11798 (2017/11/24)

Recently, contemporaneous strategies to achieve the vicinal difluorination of alkenes via an I(I)/I(III) catalysis manifold were independently reported by this laboratory and by Jacobsen and co-workers. Both strategies proceed through a transient ArI(III)

A practical synthetic method of iodoarene difluorides without fluorine gas and mercury salts

Sawaguchi, Masanori,Ayuba, Shinichi,Hara, Shoji

, p. 1802 - 1803 (2007/10/03)

Iodoarene difluorides were synthesized in three steps from the corresponding iodoarenes without the use of dangerous reagents such as fluorine gas of harmful mercury salts.

SYNTHESEN VON ARYLJOD(III)-DIFLUORIDEN DURCH DIREKTFLUORIERUNG VON ARYLJODIDEN

Naumann, D.,Ruether, G.

, p. 213 - 222 (2007/10/02)

The aryl iodides C6H5I, o-XC6H4I(X = F, I), m-FC6H4I and p-XC6H4I (X = F, Cl, Br, I, CH3, NO2) react with elemental fluorine at about -100 deg C in CCl3F to form the corresponding aryl iodine difluorides without attack on the aromatic ring.Preparations, (

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