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difluoro(4-nitrophenyl)-λ3-iodane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74953-38-1 Structure
  • Basic information

    1. Product Name: difluoro(4-nitrophenyl)-λ3-iodane
    2. Synonyms: difluoro(4-nitrophenyl)-λ3-iodane
    3. CAS NO:74953-38-1
    4. Molecular Formula:
    5. Molecular Weight: 287.005
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74953-38-1.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: difluoro(4-nitrophenyl)-λ3-iodane(CAS DataBase Reference)
    10. NIST Chemistry Reference: difluoro(4-nitrophenyl)-λ3-iodane(74953-38-1)
    11. EPA Substance Registry System: difluoro(4-nitrophenyl)-λ3-iodane(74953-38-1)
  • 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: 74953-38-1(Hazardous Substances Data)

74953-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74953-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,5 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74953-38:
(7*7)+(6*4)+(5*9)+(4*5)+(3*3)+(2*3)+(1*8)=161
161 % 10 = 1
So 74953-38-1 is a valid CAS Registry Number.

74953-38-1Downstream Products

74953-38-1Relevant articles and documents

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)

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.

Electrochemistry of Hypervalent Compounds. 6. Selective α-Fluorination of Sulfides Using Electrogenerated Hypervalent p-Methoxyiodobenzene Difluoride

Fuchigami, Toshio,Fujita, Toshiyasu,Higashiya, Seiichiro,Konno, Akinori

, p. 131 - 133 (2007/10/03)

Anodically generated hypervalent p-methoxyiodobenezene difluoride reacted with α-(arylthio)- and α-(benzylthio)acetates, and α-(phenylthio)acetophenone to provide the corresponding fluorinated compounds. In all cases, a fluorine atom was introduced exclus

Electrolytic Partial Fluorination of Organic Compounds. 14. The First Electrosynthesis of Hypervalent Iodobenzene Difluoride Derivatives and Its Application to Indirect Anodic gem-Difluorination

Fuchigami, Toshio,Fujita, Toshiyasu

, p. 7190 - 7192 (2007/10/02)

The electrosynthesis of hypervalent iodobenzene difluorides was accomplished by anodic oxidation of p-nitro- and p-methoxyiodobenzenes with Et3N*3HF in anhydrous acetonitrile, and p-methoxyiodobenzene difluoride was used as a mediator for indirect anodic

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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