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1447665-44-2

2,2,2-trifluoro-1-(4-(trityloxy)phenyl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1447665-44-2 Structure

  • Basic information

    1. Product Name: 2,2,2-trifluoro-1-(4-(trityloxy)phenyl)ethanol
    2. Synonyms:
    3. CAS NO:1447665-44-2
    4. Molecular Formula:
    5. Molecular Weight: 434.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1447665-44-2.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: 2,2,2-trifluoro-1-(4-(trityloxy)phenyl)ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2,2-trifluoro-1-(4-(trityloxy)phenyl)ethanol(1447665-44-2)
    11. EPA Substance Registry System: 2,2,2-trifluoro-1-(4-(trityloxy)phenyl)ethanol(1447665-44-2)

  • 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: 1447665-44-2(Hazardous Substances Data)

1447665-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1447665-44-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,6,6 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1447665-44:
(9*1)+(8*4)+(7*4)+(6*7)+(5*6)+(4*6)+(3*5)+(2*4)+(1*4)=192
192 % 10 = 2
So 1447665-44-2 is a valid CAS Registry Number.

1447665-44-2Upstream product

1447665-44-2Downstream Products

1447665-44-2Relevant articles and documents

Trifluoromethylation of ketones and aldehydes with Bu3SnCF 3

Sanhueza, Italo A.,Bonney, Karl J.,Nielsen, Mads C.,Schoenebeck, Franziska

, p. 7749 - 7753 (2013)

The (trifluoromethyl)stannane reagent, Bu3SnCF3, was found to react under CsF activation with ketones and aldehydes to the corresponding trifluoromethylated stannane ether intermediates at room temperature in high yield. Only a mildly acidic extraction (aqueous NH 4Cl) is required to release the corresponding trifluoromethyl alcohol products. The protocol is compatible with acid-sensitive functional groups.

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