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5-Chloro-2-ethoxypyridine-3-carboxylic acid is a pyridine derivative with the molecular formula C8H8ClNO3, featuring a chloro and ethoxy group attached to the 2 and 3 positions of the pyridine ring, respectively, along with a carboxylic acid group at the 3 position. This chemical compound is widely utilized in organic synthesis and pharmaceutical research as a versatile building block for the development of pharmaceutical drugs and biologically active compounds. Additionally, it serves as a key intermediate in the synthesis of agrochemicals, including herbicides and insecticides. Due to its potential harmful effects upon ingestion, inhalation, or contact with skin and eyes, it is crucial to adhere to proper handling and disposal procedures when working with 5-Chloro-2-ethoxypyridine-3-carboxylic acid.

68359-07-9

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68359-07-9 Usage

Uses

Used in Pharmaceutical Research and Development:
5-Chloro-2-ethoxypyridine-3-carboxylic acid is used as a building block in the synthesis of various pharmaceutical drugs and biologically active compounds. Its unique structure and functional groups make it a valuable component in the development of new medications with potential therapeutic applications.
Used in Organic Synthesis:
This chemical compound is employed as an intermediate in organic synthesis, allowing for the creation of a wide range of chemical products. Its versatility in forming different chemical bonds and its reactivity with other compounds make it a valuable asset in the field of organic chemistry.
Used in Agrochemicals:
5-Chloro-2-ethoxypyridine-3-carboxylic acid is used as a key intermediate in the synthesis of agrochemicals, such as herbicides and insecticides. Its incorporation into these products contributes to their effectiveness in controlling pests and unwanted plant growth, thereby supporting agricultural productivity and crop protection.
Used in Chemical Research:
As a pyridine derivative with unique functional groups, 5-Chloro-2-ethoxypyridine-3-carboxylic acid is utilized in chemical research to explore its properties, reactivity, and potential applications in various chemical processes and reactions. This research can lead to the discovery of new compounds and advancements in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 68359-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,5 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68359-07:
(7*6)+(6*8)+(5*3)+(4*5)+(3*9)+(2*0)+(1*7)=159
159 % 10 = 9
So 68359-07-9 is a valid CAS Registry Number.

68359-07-9Downstream Products

68359-07-9Relevant academic research and scientific papers

AN IMPROVED METHOD OF CHLORINATING 2-ALKOXYNICOTINIC ACIDS

Elliott, Mark L.,Goddard, Carl J.

, p. 1505 - 1508 (2007/10/02)

A novel chlorination process for preparing 5-chloro-2-alkoxynicotinic acids has been developed using commercial 5.25percent sodium hypochlorite (Clorox) as a chlorinating agent.

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