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2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID is a chemical compound with the molecular formula C6H2Br2F2NO2. It is a derivative of isonicotinic acid, characterized by the presence of two bromine atoms and two fluorine atoms. 2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID is recognized for its strong and selective herbicidal activity, making it a significant component in the development of agrochemicals.

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  • 325461-60-7 Structure
  • Basic information

    1. Product Name: 2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID
    2. Synonyms: 2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID;2,6-DIBROMO-3,5-DIFLUOROPYRIDINE-4-CARBOXYLIC ACID
    3. CAS NO:325461-60-7
    4. Molecular Formula: C6HBr2F2NO2
    5. Molecular Weight: 316.88
    6. EINECS: N/A
    7. Product Categories: Pyridines
    8. Mol File: 325461-60-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 398.6 °C at 760 mmHg
    3. Flash Point: 194.9 °C
    4. Appearance: /
    5. Density: 2.33 g/cm3
    6. Vapor Pressure: 4.54E-07mmHg at 25°C
    7. Refractive Index: 1.601
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. PKA: 0.73±0.10(Predicted)
    11. CAS DataBase Reference: 2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID(325461-60-7)
    13. EPA Substance Registry System: 2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID(325461-60-7)
  • 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: 325461-60-7(Hazardous Substances Data)

325461-60-7 Usage

Uses

Used in Agrochemical Industry:
2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID is used as a key intermediate in the synthesis of various pesticides and herbicides. It is valued for its effectiveness in controlling specific weed species, thereby enhancing agricultural productivity and crop protection.
Used in Pharmaceutical Synthesis:
2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID also serves as a chemical building block for the synthesis of pharmaceuticals and other organic compounds, contributing to the development of new drugs and therapeutic agents.
Environmental Considerations:
Due to its potential toxicity and environmental impact, 2,6-DIBROMO-3,5-DIFLUOROISONICOTINIC ACID requires careful handling and disposal. Proper procedures must be followed to mitigate any adverse effects on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 325461-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,4,6 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 325461-60:
(8*3)+(7*2)+(6*5)+(5*4)+(4*6)+(3*1)+(2*6)+(1*0)=127
127 % 10 = 7
So 325461-60-7 is a valid CAS Registry Number.
InChI:InChI=1/C6HBr2F2NO2/c7-4-2(9)1(6(12)13)3(10)5(8)11-4/h(H,12,13)

325461-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dibromo-3,5-difluoropyridine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names QC-7103

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:325461-60-7 SDS

325461-60-7Downstream Products

325461-60-7Relevant articles and documents

Polyhalogenated heterocyclic compounds: Part 46. Multifunctional heterocycles from bromofluoropyridine derivatives

Benmansour,Chambers,Sandford,McGowan,Dahaoui,Yufit,Howard

, p. 349 - 355 (2007/10/03)

2,4,6-Tribromo-3,5-difluoro-pyridine 1 was used as the starting material for the synthesis of a variety of multifunctional pyridine derivatives. For example, nucleophilic substitution reactions involving appropriate difunctional nucleophiles gave products resulting from intramolecular cyclisation processes and the organolithium derivative 9, readily prepared from 1, could be trapped by various of electrophilic reagents.

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