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1584705-76-9

2-(5-bromo-2-(trifluoromethylthio)phenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1584705-76-9 Structure

  • Basic information

    1. Product Name: 2-(5-bromo-2-(trifluoromethylthio)phenyl)pyridine
    2. Synonyms: 2-(5-bromo-2-(trifluoromethylthio)phenyl)pyridine
    3. CAS NO:1584705-76-9
    4. Molecular Formula:
    5. Molecular Weight: 334.159
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1584705-76-9.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-(5-bromo-2-(trifluoromethylthio)phenyl)pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(5-bromo-2-(trifluoromethylthio)phenyl)pyridine(1584705-76-9)
    11. EPA Substance Registry System: 2-(5-bromo-2-(trifluoromethylthio)phenyl)pyridine(1584705-76-9)

  • 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: 1584705-76-9(Hazardous Substances Data)

1584705-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1584705-76-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,4,7,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1584705-76:
(9*1)+(8*5)+(7*8)+(6*4)+(5*7)+(4*0)+(3*5)+(2*7)+(1*6)=199
199 % 10 = 9
So 1584705-76-9 is a valid CAS Registry Number.

1584705-76-9Downstream Products

1584705-76-9Relevant articles and documents

Palladium-catalyzed trifluoromethylthiolation of aryl C-H bonds

Xu, Chunfa,Shen, Qilong

supporting information, p. 2046 - 2049 (2014/05/06)

A method for monotrifluoromethylthiolation of arenes via palladium-catalyzed directed C-H bond activation was described. The reaction was compatible with a variety of functional groups. Initial mechanistic studies disclosed that the turnover limiting step of the catalytic cycle did not involve C-H activation.

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