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CAS

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1446753-59-8

4-(benzyloxydimethylsilyl)butylferrocene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446753-59-8 Structure

  • Basic information

    1. Product Name: 4-(benzyloxydimethylsilyl)butylferrocene
    2. Synonyms: 4-(benzyloxydimethylsilyl)butylferrocene
    3. CAS NO:1446753-59-8
    4. Molecular Formula:
    5. Molecular Weight: 406.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446753-59-8.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: 4-(benzyloxydimethylsilyl)butylferrocene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(benzyloxydimethylsilyl)butylferrocene(1446753-59-8)
    11. EPA Substance Registry System: 4-(benzyloxydimethylsilyl)butylferrocene(1446753-59-8)

  • 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: 1446753-59-8(Hazardous Substances Data)

1446753-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446753-59-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,7,5 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1446753-59:
(9*1)+(8*4)+(7*4)+(6*6)+(5*7)+(4*5)+(3*3)+(2*5)+(1*9)=188
188 % 10 = 8
So 1446753-59-8 is a valid CAS Registry Number.

1446753-59-8Downstream Products

1446753-59-8Relevant articles and documents

Synthesis of novel ferrocenyl silyl ethers via dehydrocoupling reactions under Karstedt catalyst

Safa, Kazem D.,Abbasi, Hassan,Teimuri-Mofrad, Reza

, p. 56 - 60 (2013)

Abstract (4-Ferrocenylbutyl)dimethylsilane is prepared by a Grignard reaction from 4-chlorobutylferrocene and chlorodimethylsilane in THF. The Si-H group reacts with primary and secondary alcohols at room temperature to give good yields of (4-ferrocenylbutyl)dimethylsilyl ethers with Karstedt catalyst in THF. Ferrocenyl groups in pendant side chain are attached to cellulose acetate butyrate via alcoholysis at room temperature with Karstedt catalyst.

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