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bis(4-iodophenyl)methyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103897-56-9 Structure
  • Basic information

    1. Product Name: bis(4-iodophenyl)methyl ether
    2. Synonyms:
    3. CAS NO:103897-56-9
    4. Molecular Formula:
    5. Molecular Weight: 854.046
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103897-56-9.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: bis(4-iodophenyl)methyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis(4-iodophenyl)methyl ether(103897-56-9)
    11. EPA Substance Registry System: bis(4-iodophenyl)methyl ether(103897-56-9)
  • 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: 103897-56-9(Hazardous Substances Data)

103897-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103897-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,9 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103897-56:
(8*1)+(7*0)+(6*3)+(5*8)+(4*9)+(3*7)+(2*5)+(1*6)=139
139 % 10 = 9
So 103897-56-9 is a valid CAS Registry Number.

103897-56-9Downstream Products

103897-56-9Relevant articles and documents

CARBOXYLATION OF ALCOHOLS WITH CARBON MONOXIDE SUPERSATURATED IN STRONG ACID. FACILE SYNTHESIS OF 2,2-BIS(4-HALOPHENYL)ACETIC, -PROPIONIC, AND RELATED ACIDS

Takahashi, Yukio,Yoneda, Norihiko,Nagai, Hiroshi

, p. 1733 - 1734 (2007/10/02)

Using 97percent H2SO4 supersaturated with carbon monoxide, bis(4-halophenyl)methanols, 1,1-bis(4-halophenyl)ethanols and related alcohols were transformed to the carboxylic acids in 60-95percent yields.

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