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CAS

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101089-30-9

1-(2-iodo-1-phenylethyl)-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101089-30-9 Structure

  • Basic information

    1. Product Name: 1-(2-iodo-1-phenylethyl)-4-methoxybenzene
    2. Synonyms: 1-(2-iodo-1-phenylethyl)-4-methoxybenzene
    3. CAS NO:101089-30-9
    4. Molecular Formula:
    5. Molecular Weight: 338.188
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101089-30-9.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: 1-(2-iodo-1-phenylethyl)-4-methoxybenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-iodo-1-phenylethyl)-4-methoxybenzene(101089-30-9)
    11. EPA Substance Registry System: 1-(2-iodo-1-phenylethyl)-4-methoxybenzene(101089-30-9)

  • 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: 101089-30-9(Hazardous Substances Data)

101089-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101089-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,8 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101089-30:
(8*1)+(7*0)+(6*1)+(5*0)+(4*8)+(3*9)+(2*3)+(1*0)=79
79 % 10 = 9
So 101089-30-9 is a valid CAS Registry Number.

101089-30-9Downstream Products

101089-30-9Relevant articles and documents

Samarium triflate-catalyzed halogen-promoted Friedel-Crafts alkylation with alkenes

Hajra, Saumen,Maji, Biswajit,Bar, Sukanta

, p. 2783 - 2786 (2008/02/05)

A versatile and efficient halogen-promoted highly regio- and stereoselective Friedel - Crafts (F-C) alkylation with alkenes has been developed with use of easily available and inexpensive NBS or I2 as the efficient halogen sources. Lewis acids, in particular metal triflates, are found to be effective catalysts for this halogen-promoted F-C alkylation. Among these, Sm(OTf)3 was the best catalyst. Electron-rich arenes smoothly underwent F-C alkylation with a variety of alkenes including α,β-unsaturated carbonyl compounds.

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