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505084-58-2

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505084-58-2 Usage

Description

2-Chloro-5-(trifluoromethyl)isonicotinic acid 97% is a chemical compound that belongs to the family of isonicotinic acids. It is characterized by the presence of a chlorine atom at the 2nd position and a trifluoromethyl group at the 5th position of the isonicotinic acid structure. 2-Chloro-5-(trifluoromethyl)isonicotinic acid 97% is typically available in a purity of 97%, making it a valuable intermediate for various applications in the pharmaceutical, organic synthesis, and organic light-emitting diode (OLED) industries.

Uses

Used in Pharmaceutical Industry:
2-Chloro-5-(trifluoromethyl)isonicotinic acid 97% is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a key building block in the development of new drugs, particularly those targeting specific receptors or enzymes in the human body.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Chloro-5-(trifluoromethyl)isonicotinic acid 97% serves as a versatile intermediate for the creation of a wide range of organic compounds. Its reactivity and functional groups make it a valuable component in the synthesis of various molecules, including those with potential applications in materials science, agrochemicals, and other specialty chemicals.
Used in Organic Light-Emitting Diode (OLED) Industry:
2-Chloro-5-(trifluoromethyl)isonicotinic acid 97% is also utilized as a key intermediate in the development of organic light-emitting diode (OLED) materials. OLEDs are widely used in display technologies, such as televisions, smartphones, and other electronic devices, due to their high efficiency, thin and lightweight design, and ability to produce vibrant colors. 2-Chloro-5-(trifluoromethyl)isonicotinic acid 97%'s properties make it an essential component in the design and synthesis of new OLED materials with improved performance and durability.

Check Digit Verification of cas no

The CAS Registry Mumber 505084-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,5,0,8 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 505084-58:
(8*5)+(7*0)+(6*5)+(5*0)+(4*8)+(3*4)+(2*5)+(1*8)=132
132 % 10 = 2
So 505084-58-2 is a valid CAS Registry Number.

505084-58-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H64361)  2-Chloro-5-(trifluoromethyl)pyridine-4-carboxylic acid, 97%   

  • 505084-58-2

  • 250mg

  • 214.0CNY

  • Detail
  • Alfa Aesar

  • (H64361)  2-Chloro-5-(trifluoromethyl)pyridine-4-carboxylic acid, 97%   

  • 505084-58-2

  • 1g

  • 642.0CNY

  • Detail
  • Alfa Aesar

  • (H64361)  2-Chloro-5-(trifluoromethyl)pyridine-4-carboxylic acid, 97%   

  • 505084-58-2

  • 5g

  • 2568.0CNY

  • Detail

505084-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-5-(Trifluoromethyl)Isonicotinic Acid

1.2 Other means of identification

Product number -
Other names 2-chloro-5-(trifluoromethyl)pyridine-4-carboxylic acid

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:505084-58-2 SDS

505084-58-2Relevant articles and documents

Three chloro(trifluoromethyl)pyridines as model substrates for regioexhaustive functionalization

Cottet, Fabrice,Schlosser, Manfred

, p. 3793 - 3798 (2007/10/03)

As a further test of the concept of regioexhaustive functionalization, 2-chloro-6-(trifluoromethyl)pyridine, 2-chloro-5-(trifluoromethyl)pyridine and 3-chloro-4-(trifluoromethyl)-pyridine were each converted into the three possible carboxylic acids 2, 4, 6, 8, 10, 12, 16, 17 and 20. This was achieved by employing several, but not all of the organometallic "tool-box methods": transformation of a more basic organometallic species into a less basic isomer by transmetalation-equilibration, site discriminating deprotonation with lithium N,N-diisopropylamide or lithium 2,2,6,6- tetramethylpiperidide, regio-divergent iodine migration and steric screening of acidic positions by a bulky trialkylsilyl group. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

New strategies in the synthesis of regioselectively trifluoromethyl- and trifluoromethoxy-substituted arenes as building blocks for biologically active molecules

Leconte, Stephane,Ruzziconi, Renzo

, p. 167 - 172 (2007/10/03)

Regioisomerically pure trifluoromethyl- and trifluoromethoxy-substituted aromatic and heteroaromatic aldehydes and carboxylic acids are valuable building blocks for the synthesis of biologically active molecules. They have been prepared by employing moder

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