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347-82-0

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347-82-0 Usage

General Description

Phenol, 4-fluoro-, 4-nitrobenzoate is a chemical compound containing phenol, fluorine, and nitro groups attached to a benzene ring. It is commonly used in organic synthesis and as a building block for the production of pharmaceuticals, dyes, and agrochemicals. Phenol, 4-fluoro-, 4-nitrobenzoate exhibits various biological activities and has been studied for its potential use in the treatment of diseases such as cancer and inflammation. Its unique combination of functional groups makes it a versatile molecule for diverse applications in the field of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 347-82-0 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 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 347-82:
(5*3)+(4*4)+(3*7)+(2*8)+(1*2)=70
70 % 10 = 0
So 347-82-0 is a valid CAS Registry Number.

347-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-benzoic acid-(4-fluoro-phenyl ester)

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzoesaeure-(4-fluor-phenylester)

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:347-82-0 SDS

347-82-0Relevant articles and documents

Decarboxylative Hydroxylation of Benzoic Acids

Ritter, Tobias,Su, Wanqi,Xu, Peng

supporting information, p. 24012 - 24017 (2021/10/06)

Herein, we report the first decarboxylative hydroxylation to synthesize phenols from benzoic acids at 35 °C via photoinduced ligand-to-metal charge transfer (LMCT)-enabled radical decarboxylative carbometalation. The aromatic decarboxylative hydroxylation is synthetically promising due to its mild conditions, broad substrate scope, and late-stage applications.

Studies in organic fluorine compounds. Synthesis of fluorinated hydrazones, aryl esters of p halogenated phenols, fluorinated hydroxy ketones and their thiosemicarbazones and fluoro substituted thiazoles and their derivatives as possible fungicides

Srivastava,Bahel

, p. 841 - 845 (2007/10/10)

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