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174518-80-0

Benzene, 1,5-diiodo-2,3,4-trimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 174518-80-0 Structure

  • Basic information

    1. Product Name: Benzene, 1,5-diiodo-2,3,4-trimethoxy-
    2. Synonyms:
    3. CAS NO:174518-80-0
    4. Molecular Formula: C9H10I2O3
    5. Molecular Weight: 419.986
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174518-80-0.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: Benzene, 1,5-diiodo-2,3,4-trimethoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1,5-diiodo-2,3,4-trimethoxy-(174518-80-0)
    11. EPA Substance Registry System: Benzene, 1,5-diiodo-2,3,4-trimethoxy-(174518-80-0)

  • 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: 174518-80-0(Hazardous Substances Data)

174518-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174518-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,5,1 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 174518-80:
(8*1)+(7*7)+(6*4)+(5*5)+(4*1)+(3*8)+(2*8)+(1*0)=150
150 % 10 = 0
So 174518-80-0 is a valid CAS Registry Number.

174518-80-0Downstream Products

174518-80-0Relevant articles and documents

Hypervalent iodine(III)-LiX combination in fluoroalcohol solvent for aromatic halogenation of electron-rich arenecarboxylic acids

Hamamoto, Hiromi,Hattori, Sho,Takemaru, Kaori,Miki, Yasuyoshi

scheme or table, p. 1563 - 1566 (2011/08/03)

The novel reagent system, PhI(OAc)2-LiX combination in fluoroalcohol solvents, was found to be effective for halodecarboxylation of electron-rich arenecarboxylic acids. The method provided an efficient route to halogenated phenol ether derivatives. Georg Thieme Verlag Stuttgart ? New York.

Iodination of alkyl aryl ethers by mercury(II) oxide-iodine reagent in dichloromethane

Orito,Hatakeyama,Takeo,Suginome

, p. 1273 - 1277 (2007/10/02)

A convenient method for selective mono- and diiodination of alkyl aryl ethers by mercury(II) oxide-iodine reagent in dichloromethane is reported.

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