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343-72-6

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343-72-6 Usage

General Description

3-Fluoropyridine-4-carboxylic acid ethyl ester is a chemical compound with the molecular formula C8H7NO2F. It is an ester of the 3-fluoropyridine-4-carboxylic acid, commonly used as a building block in organic synthesis and pharmaceutical research. 3-Fluoropyridine-4-carboxylic acid ethyl ester is commonly utilized in the development of drugs and agrochemicals due to its potential biological activities. It is also used as an intermediate in the synthesis of various pharmaceutical compounds and has applications in the manufacturing of various products in the pharmaceutical and chemical industries.

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 articles and documents

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.

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