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CAS

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509072-60-0

1-(2,2-difluorocyclopropyl)ethyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 509072-60-0 Structure

  • Basic information

    1. Product Name: 1-(2,2-difluorocyclopropyl)ethyl benzoate
    2. Synonyms:
    3. CAS NO:509072-60-0
    4. Molecular Formula:
    5. Molecular Weight: 226.223
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 509072-60-0.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: 1-(2,2-difluorocyclopropyl)ethyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2,2-difluorocyclopropyl)ethyl benzoate(509072-60-0)
    11. EPA Substance Registry System: 1-(2,2-difluorocyclopropyl)ethyl benzoate(509072-60-0)

  • 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: 509072-60-0(Hazardous Substances Data)

509072-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 509072-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,9,0,7 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 509072-60:
(8*5)+(7*0)+(6*9)+(5*0)+(4*7)+(3*2)+(2*6)+(1*0)=140
140 % 10 = 0
So 509072-60-0 is a valid CAS Registry Number.

509072-60-0Relevant articles and documents

Reactivity and regiochemical behavior in the solvolysis reactions of (2,2-difluorocyclopyl)methyl tosylates

Battiste, Merle A.,Tian, Feng,Baker, John M.,Bautista, Olivia,Villalobos, Janette,Dolbier Jr., William R.

, p. 39 - 51 (2007/10/03)

The rate constants for acetolysis of (2,2-difluorocyclopropyl)methyl tosylate, and (2,2-difluoro-3-methylcyclopropyl)methyl tosylate at 92°C and of 1-(2,2-difluoropropyl)ethyl tosylate at 42°C are reported and the rectivities and regiochemistries of ring opening of these systems are discussed and compared with expectations based on computational results. The results are discussed in terms of the use of (2,2-difluorocyclopropyl)methyl systems as mechanistic probes.

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