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4-Bromo-2,3,5-trifluoropyridine is a halogenated pyridine derivative with the molecular formula C5H3BrF3N. It is known for its strong electron-withdrawing properties due to the presence of both bromine and fluorine atoms, making it a useful reagent in the formation of C-C and C-N bonds.

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  • 851178-96-6 Structure
  • Basic information

    1. Product Name: 4-Bromo-2,3,5-trifluoropyridine
    2. Synonyms: 4-bromo-2,3,5-trifluoropyridine(WXFC0751)
    3. CAS NO:851178-96-6
    4. Molecular Formula: C5H2F3N
    5. Molecular Weight: 211.97
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 851178-96-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 158.2°C at 760 mmHg
    3. Flash Point: 49.5°C
    4. Appearance: /
    5. Density: 1.901g/cm3
    6. Vapor Pressure: 3.43mmHg at 25°C
    7. Refractive Index: 1.486
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: -1.44±0.10(Predicted)
    11. CAS DataBase Reference: 4-Bromo-2,3,5-trifluoropyridine(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-Bromo-2,3,5-trifluoropyridine(851178-96-6)
    13. EPA Substance Registry System: 4-Bromo-2,3,5-trifluoropyridine(851178-96-6)
  • 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: 851178-96-6(Hazardous Substances Data)

851178-96-6 Usage

Uses

Used in Organic Synthesis:
4-Bromo-2,3,5-trifluoropyridine is used as a building block in organic synthesis for its strong electron-withdrawing properties, which facilitate the formation of C-C and C-N bonds.
Used in Pharmaceutical Research:
4-Bromo-2,3,5-trifluoropyridine is used as a key intermediate in the synthesis of various bioactive molecules in pharmaceutical research.
Used in Agrochemical Research:
4-Bromo-2,3,5-trifluoropyridine is used as a key intermediate in the synthesis of bioactive molecules in agrochemical research.
Used in Materials Science:
4-Bromo-2,3,5-trifluoropyridine is used in the development of organic light-emitting diodes (OLEDs) and other electronic devices in materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 851178-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,1,7 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 851178-96:
(8*8)+(7*5)+(6*1)+(5*1)+(4*7)+(3*8)+(2*9)+(1*6)=186
186 % 10 = 6
So 851178-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C5HBrF3N/c6-3-2(7)1-10-5(9)4(3)8/h1H

851178-96-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-2,3,5-trifluoropyridine

1.2 Other means of identification

Product number -
Other names PC9693

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:851178-96-6 SDS

851178-96-6Downstream Products

851178-96-6Relevant articles and documents

Removal of fluorine from and introduction of fluorine into polyhalopyridines: An exercise in nucleophilic hetarenic substitution

Bobbio, Carla,Rausis, Thierry,Schlosser, Manfred

, p. 1903 - 1910 (2005)

Starting from six industrially available fluorinated pyridines, an expedient access to all three tetrafluoropyridines (2-4), all six trifluoropyridines (5-10), and the five non-commercial difluoropyridines (11-14 and 16) was developed. The methods employed for the selective removal of fluorine from polyfluoropyridines were the reduction by metals or complex hydrides and the site-selective replacement by hydrazine followed by dehydrogenation-dediazotation or dehydrochlorination-dediazotation. To introduce an extra fluorine atom, a suitable precursor was metalated and chlorinated before being subjected to a chlorine/ fluorine displacement process.

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