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CAS

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1648827-66-0

6,6,6-trifluoro-3-oxohexyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1648827-66-0 Structure

  • Basic information

    1. Product Name: 6,6,6-trifluoro-3-oxohexyl benzoate
    2. Synonyms:
    3. CAS NO:1648827-66-0
    4. Molecular Formula:
    5. Molecular Weight: 274.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1648827-66-0.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: 6,6,6-trifluoro-3-oxohexyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,6,6-trifluoro-3-oxohexyl benzoate(1648827-66-0)
    11. EPA Substance Registry System: 6,6,6-trifluoro-3-oxohexyl benzoate(1648827-66-0)

  • 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: 1648827-66-0(Hazardous Substances Data)

1648827-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1648827-66-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,8,8,2 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1648827-66:
(9*1)+(8*6)+(7*4)+(6*8)+(5*8)+(4*2)+(3*7)+(2*6)+(1*6)=220
220 % 10 = 0
So 1648827-66-0 is a valid CAS Registry Number.

1648827-66-0Upstream product

1648827-66-0Downstream Products

1648827-66-0Relevant articles and documents

Rapid access to β-trifluoromethyl-substituted ketones: Harnessing inductive effects in wacker-type oxidations of internal alkenes

Lerch, Michael M.,Morandi, Bill,Wickens, Zachary K.,Grubbs, Robert H.

, p. 8654 - 8658 (2014)

We present a practical trifluoromethyl-directed Wacker-type oxidation of internal alkenes that enables rapid access to β-trifluoromethyl-substituted ketones. Allylic trifluoromethyl-substituted alkenes bearing a wide range of functional groups can be oxidized in high yield and regioselectivity. The distance dependence of the regioselectivity was established by systematic variation of the number of methylene units between the double bond and the trifluoromethyl group. The regioselectivity enforced by traditional directing groups could even be reversed by introduction of a competing trifluoromethyl group. Besides being a new powerful synthetic method to prepare fluorinated molecules, this work directly probes the role of inductive effects on nucleopalladation events.

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