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3-Fluoropyridine-4-carboxylic acid ethyl ester is a chemical compound with the molecular formula C8H7NO2F. It is an ester of 3-fluoropyridine-4-carboxylic acid, characterized by the presence of a fluorine atom at the 3-position and an ethyl ester group at the 4-position of the pyridine ring. 3-Fluoropyridine-4-carboxylic acid ethyl ester is widely used as a building block in organic synthesis and pharmaceutical research due to its unique structural features and potential biological activities.

343-72-6

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343-72-6 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
3-Fluoropyridine-4-carboxylic acid ethyl ester is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence in the molecular structure of drugs can impart specific biological activities, such as improved binding affinity, selectivity, and pharmacokinetic properties. This makes it a valuable component in the development of new drugs with enhanced therapeutic effects and reduced side effects.
Used in Agrochemical Development:
3-Fluoropyridine-4-carboxylic acid ethyl ester is also utilized in the development of agrochemicals, such as pesticides and herbicides. Its incorporation into the molecular structure of these chemicals can enhance their efficacy in controlling pests and weeds, while minimizing the environmental impact and potential harm to non-target organisms.
Used in Organic Synthesis:
As a versatile building block, 3-Fluoropyridine-4-carboxylic acid ethyl ester is employed in various organic synthesis processes. Its reactivity and functional groups allow for the formation of a wide range of chemical derivatives, which can be further used in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Manufacturing Processes:
3-Fluoropyridine-4-carboxylic acid ethyl ester finds applications in the manufacturing of various products in the pharmaceutical and chemical industries. Its use as an intermediate in the synthesis of pharmaceutical compounds contributes to the production of life-saving drugs and medicines. Additionally, its role in the synthesis of agrochemicals and other specialty chemicals supports the development of innovative products that address various challenges in agriculture, healthcare, and other sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 343-72-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 343-72:
(5*3)+(4*4)+(3*3)+(2*7)+(1*2)=56
56 % 10 = 6
So 343-72-6 is a valid CAS Registry Number.

343-72-6SDS

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 ethyl 3-fluoropyridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Fluor-isonicotinsaeure-aethylester

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:343-72-6 SDS

343-72-6Downstream Products

343-72-6Relevant academic research and scientific papers

Hypervalent Iodine(III)-Catalyzed Balz–Schiemann Fluorination under Mild Conditions

Xing, Bo,Ni, Chuanfa,Hu, Jinbo

, p. 9896 - 9900 (2018/07/31)

An unprecedented hypervalent iodine(III) catalyzed Balz–Schiemann reaction is described. In the presence of a hypervalent iodine compound, the fluorination reaction proceeds under mild conditions (25–60 °C), and features a wide substrate scope and good functional-group compatibility.

AMINO-TETRAZOLES ANALOGUES AND METHODS OF USE

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Page/Page column 156, (2010/02/14)

A compound having Formula (I) or Formula (II) is disclosed as an P2X7 antagonist, wherein A, B, C, Y, Y, Z, m, v, R1, R2, R3, R4, and R 5, are as defined in the description. Methods and compositions for treating disease or condition modulated by P2X7 are also disclosed.

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