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2-fluoro-6-(4-fluorophenyl)pyridine is a chemical compound with a molecular formula C11H7FN2. It is a pyridine derivative featuring a fluoro group at the 2-position and a 4-fluorophenyl group attached to the 6-position. 2-fluoro-6-(4-fluorophenyl)pyridine is recognized for its unique structure and reactivity, which makes it a valuable intermediate in organic chemistry for the synthesis of complex molecules. The presence of fluoro substituents endows it with increased stability and modified electronic properties, contributing to its utility in the development of pharmaceuticals, agrochemicals, and new materials.

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  • 180606-14-8 Structure
  • Basic information

    1. Product Name: 2-fluoro-6-(4-fluorophenyl)pyridine
    2. Synonyms: 2-fluoro-6-(4-fluorophenyl)pyridine
    3. CAS NO:180606-14-8
    4. Molecular Formula: C11H7F2N
    5. Molecular Weight: 191.1767864
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 180606-14-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 278.8±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.222±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: -1.16±0.25(Predicted)
    10. CAS DataBase Reference: 2-fluoro-6-(4-fluorophenyl)pyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-fluoro-6-(4-fluorophenyl)pyridine(180606-14-8)
    12. EPA Substance Registry System: 2-fluoro-6-(4-fluorophenyl)pyridine(180606-14-8)
  • 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: 180606-14-8(Hazardous Substances Data)

180606-14-8 Usage

Uses

Used in Pharmaceutical Synthesis:
2-fluoro-6-(4-fluorophenyl)pyridine is utilized as a key building block in the creation of various pharmaceutical agents. Its specific structural features and reactivity facilitate the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Development:
In the agrochemical industry, 2-fluoro-6-(4-fluorophenyl)pyridine serves as an essential intermediate for the synthesis of pesticides and other crop protection agents. Its properties contribute to the enhancement of the stability and activity of these compounds, ensuring more effective agricultural solutions.
Used in Organic Chemistry Research:
As a versatile intermediate, 2-fluoro-6-(4-fluorophenyl)pyridine is employed in organic chemistry research for exploring novel synthetic pathways and developing innovative methodologies. Its unique attributes make it a promising candidate for the construction of complex organic molecules and the study of reaction mechanisms.
Used in Material Science:
2-fluoro-6-(4-fluorophenyl)pyridine's fluoro substituents and electronic characteristics make 2-fluoro-6-(4-fluorophenyl)pyridine a candidate for use in material science, where it can be incorporated into the design of new materials with tailored properties for specific applications, such as in electronics or advanced coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 180606-14-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,0 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 180606-14:
(8*1)+(7*8)+(6*0)+(5*6)+(4*0)+(3*6)+(2*1)+(1*4)=118
118 % 10 = 8
So 180606-14-8 is a valid CAS Registry Number.

180606-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-6-(4-fluorophenyl)pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2-fluoro-6-(4-fluorophenyl)

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:180606-14-8 SDS

180606-14-8Downstream Products

180606-14-8Relevant articles and documents

NOVEL COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF INFLAMMATORY DISORDERS

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Paragraph 00392; page 164, (2015/01/07)

The present invention discloses compounds according to Formula I: Wherein R 1a, R 1b, R 2, R 4, R5, R 6, R 7, R 8, W, X, Y, Z, Cy, and the subscript a are as defined h

Herbicidal 2-(hectero)aryloxy-6-arypyridines and 2-aryl-4-(hetero)aryloxypyrimidines

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, (2008/06/13)

New herbicidal pyridine and pyrimidine derivatives of general formula (I), STR1 wherein Z represents a nitrogen atom or a C--H group; A represents an optionally substituted aryl group or an optionally substituted 5- or 6-membered nitrogen-containing heteroaromatic group; n represents an integer from 0 to 2 and R1 or each R1 independently represents a hydrogen atom or an optionally substituted alkyl, alkoxy, alkylthio or dialkylamino group; m represents an integer from 0 to 5 and R2 or each R2 independently represents a hydrogen or a halogen atom or an optionally substituted alkyl, haloalkyl, haloalkoxy, alkoxy, alkylthio group or a nitro, cyano or a halosulphonyl group; and X represents an oxygen or sulphur atom.

Herbicidal 2, 6-disubstituted pyridines and 2, 4-disubstituted pyrimidines

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, (2008/06/13)

New herbicidal pyrimidine derivatives of general formula (I), STR1 wherein Z represents a nitrogen atom; A represents a substituted aryl group or an optionally substituted pyridyl or pyrazolyl group; n represents an integer from 0 to 2 and R1 or each R1 independently represents a hydrogen atom or an optionally substituted alkyl, alkoxy, alkylthio or dialkylamino group; m represents an integer from 0 to 5 and R2 or each R2 independently represents a hydrogen or a halogen atom or an optionally substituted alkyl, haloalkyl, haloalkoxy, alkoxy, alkylthio group or a nitro, cyano or a halosulphonyl group; and X represents an oxygen or sulphur atom.

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