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860611-86-5

1-(2-HYDROXY-4-([3-(TRIFLUOROMETHYL)BENZYL]OXY)PHENYL)-1-ETHANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 860611-86-5 Structure

  • Basic information

    1. Product Name: 1-(2-HYDROXY-4-([3-(TRIFLUOROMETHYL)BENZYL]OXY)PHENYL)-1-ETHANONE
    2. Synonyms: 1-(2-HYDROXY-4-([3-(TRIFLUOROMETHYL)BENZYL]OXY)PHENYL)-1-ETHANONE
    3. CAS NO:860611-86-5
    4. Molecular Formula: C16H13F3O3
    5. Molecular Weight: 310.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 860611-86-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(2-HYDROXY-4-([3-(TRIFLUOROMETHYL)BENZYL]OXY)PHENYL)-1-ETHANONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-HYDROXY-4-([3-(TRIFLUOROMETHYL)BENZYL]OXY)PHENYL)-1-ETHANONE(860611-86-5)
    11. EPA Substance Registry System: 1-(2-HYDROXY-4-([3-(TRIFLUOROMETHYL)BENZYL]OXY)PHENYL)-1-ETHANONE(860611-86-5)

  • 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: 860611-86-5(Hazardous Substances Data)

860611-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 860611-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,0,6,1 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 860611-86:
(8*8)+(7*6)+(6*0)+(5*6)+(4*1)+(3*1)+(2*8)+(1*6)=165
165 % 10 = 5
So 860611-86-5 is a valid CAS Registry Number.

860611-86-5Downstream Products

860611-86-5Relevant articles and documents

Natural Products as Sources of New Fungicides (I): Synthesis and Antifungal Activity of Acetophenone Derivatives Against Phytopathogenic Fungi

Ma, Ya-Tuan,Fan, Hua-Fang,Gao, Yu-Qi,Li, He,Zhang, An-Ling,Gao, Jin-Ming

, p. 545 - 552 (2013/06/05)

Several series of 45 acetophenone derivatives bearing various alkyl or benzyl substituents were conveniently synthesized and their structures characterized by 1H and 13C NMR spectroscopy, HRMS and single-crystal X-ray analysis. Their in vitro antifungal activities against a panel of phytopathogenic fungi were evaluated by mycelial growth rate assay. Of them, 12 derivatives (e.g., 3a-c, 4c and 4e) exhibited more potent antifungal effects on some phytopathogens than a commercial fungicide hymexazol as positive control. In particular, compound 3b with IC50 values of 10-19μg/mL was found to be the most active in this series and might be a potential lead structure for further optimization. The preliminary structure-activity relationship (SAR) studies of a series of acetophenones are also discussed. A series of acetophenone derivatives have been synthesized and tested for their antifungal activities. Of them 12 derivatives exhibited more potent antifungal effects on some phytopathogens than a positive control hymexazol. Especially, compound 3b (IC50=10-19μg/mL) was found to be the most active and might be a potential lead structure. The SAR of these acetophenones is also discussed.

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