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3-bromo-2-(trifluoromethoxy)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1086393-00-1 Structure
  • Basic information

    1. Product Name: 3-bromo-2-(trifluoromethoxy)pyridine
    2. Synonyms: 3-bromo-2-(trifluoromethoxy)pyridine
    3. CAS NO:1086393-00-1
    4. Molecular Formula: C6H3BrF3NO
    5. Molecular Weight: 241.9933296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1086393-00-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 151.6±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.737±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    8. Solubility: N/A
    9. PKA: -2.54±0.29(Predicted)
    10. CAS DataBase Reference: 3-bromo-2-(trifluoromethoxy)pyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-bromo-2-(trifluoromethoxy)pyridine(1086393-00-1)
    12. EPA Substance Registry System: 3-bromo-2-(trifluoromethoxy)pyridine(1086393-00-1)
  • 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: 1086393-00-1(Hazardous Substances Data)

1086393-00-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1086393-00-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,3,9 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1086393-00:
(9*1)+(8*0)+(7*8)+(6*6)+(5*3)+(4*9)+(3*3)+(2*0)+(1*0)=161
161 % 10 = 1
So 1086393-00-1 is a valid CAS Registry Number.

1086393-00-1Downstream Products

1086393-00-1Relevant articles and documents

Regioselective Synthesis of N-Heteroaromatic Trifluoromethoxy Compounds by Direct O-CF3 Bond Formation

Liang, Apeng,Han, Shuaijun,Liu, Zhenwei,Wang, Liang,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng

supporting information, p. 5102 - 5106 (2016/04/09)

The first one-step method for the synthesis of ortho-N-heteroaromatic trifluoromethoxy derivatives by site-specific O-CF3 bond formation using hydroxylated N-heterocycles and Togni's reagent is described. The approach enables the unprecedented syntheses of a wide range of six or five-membered N-heteroaromatic trifluoromethoxy compounds containing one or two heteroatoms from most commonly used hydroxylated N-heterocycles. Notable advantages of this method include its simplicity and mild conditions, avoidance of the need for metals or toxic reagents, and compatibility with a variety of functional groups. Furthermore, this method is especially suitable for the larger scale application.

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