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82671-02-1

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82671-02-1 Usage

Description

2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile is a pyridine derivative, characterized as a fluorinated heterocyclic building block utilized in chemical synthesis. It presents itself as a light yellow crystalline powder, indicating its potential for use in various chemical processes due to its distinct structural features.

Uses

Used in Pharmaceutical Industry:
2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile serves as an intermediate in the synthesis of pharmaceutical compounds. Its unique molecular structure, including the presence of fluorine and chlorine atoms, makes it a valuable component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile is used as a precursor in the production of pesticides and other crop protection agents. Its chemical properties allow for the creation of compounds that can effectively manage pests and diseases in agriculture, contributing to increased crop yields and food security.
Used in Chemical Research:
2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile is also utilized in academic and industrial research settings. It is employed as a building block for the synthesis of novel heterocyclic compounds, which can be explored for their potential applications in various fields, including materials science, medicinal chemistry, and environmental chemistry.
Used in Material Science:
2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile finds application in material science as a component in the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of substances with tailored characteristics, such as improved stability, reactivity, or selectivity, which can be beneficial in a range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 82671-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,7 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82671-02:
(7*8)+(6*2)+(5*6)+(4*7)+(3*1)+(2*0)+(1*2)=131
131 % 10 = 1
So 82671-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl2FNO2/c7-4-2(6(11)12)1-3(9)5(8)10-4/h1H,(H,11,12)

82671-02-1 Well-known Company Product Price

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  • TCI America

  • (D3972)  2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile  >98.0%(GC)

  • 82671-02-1

  • 5g

  • 395.00CNY

  • Detail
  • TCI America

  • (D3972)  2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile  >98.0%(GC)

  • 82671-02-1

  • 25g

  • 1,250.00CNY

  • Detail
  • Alfa Aesar

  • (H26747)  2,6-Dichloro-3-cyano-5-fluoropyridine, 98%   

  • 82671-02-1

  • 5g

  • 410.0CNY

  • Detail
  • Alfa Aesar

  • (H26747)  2,6-Dichloro-3-cyano-5-fluoropyridine, 98%   

  • 82671-02-1

  • 25g

  • 1264.0CNY

  • Detail
  • Aldrich

  • (422169)  2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile  98%

  • 82671-02-1

  • 422169-25G

  • 2,688.66CNY

  • Detail

82671-02-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile

1.2 Other means of identification

Product number -
Other names 2,6-dichloro-5-fluoropyridine-3-carbonitrile

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:82671-02-1 SDS

82671-02-1Relevant articles and documents

Process for the preparation of nicotinic acids

-

, (2008/06/13)

The present invention relates to an improved process for the preparation of nicotinic acids represented by the following structural formula (I): STR1 which are prepared by reacting a nicotinic amide compound having the formula: STR2 under acidic conditions with a nitrite salt. In the process of the invention have the groups R1, R2, and R3, in the compounds are independently selected from the group consisting of hydrogen, and halogen atoms and R4 is selected from the group consisting of hydrogen, lower alkyl and aryl. The process provides the nicotinic acid compounds in improved yields.

Pyridonecarboxylic acids as antibacterial agents. VIII. An alternative synthesis of enoxacin via fluoronicotinic acid derivatives

Miyamoto,Egawa,Matsumoto

, p. 2280 - 2285 (2007/10/02)

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