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2,3,5,6-tetrafluoro-4-nitrobenzonitrile is a chemical compound with the molecular formula C7H1N2O2F4. It is an organic compound that consists of a benzene ring with four fluorine atoms and a nitro group attached to it, as well as a nitrile functional group. 2,3,5,6-tetrafluoro-4-nitrobenzonitrile is known for its reactivity and is commonly used as an intermediate in the synthesis of other organic compounds, particularly in the pharmaceutical and agrochemical industries.

17823-35-7

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17823-35-7 Usage

Uses

Used in Pharmaceutical Industry:
2,3,5,6-tetrafluoro-4-nitrobenzonitrile is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications, making it a valuable component in drug development.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3,5,6-tetrafluoro-4-nitrobenzonitrile is employed as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity enables the formation of compounds with specific properties that can be tailored to target pests or weeds effectively.
Used in Chemical Research:
2,3,5,6-tetrafluoro-4-nitrobenzonitrile is also utilized in academic and industrial research settings as a model compound for studying the effects of fluorination and nitration on the reactivity and properties of organic molecules. This helps in understanding the fundamental principles of organic chemistry and can lead to the discovery of new synthetic pathways and applications.
Safety Considerations:
Due to its highly reactive nature, 2,3,5,6-tetrafluoro-4-nitrobenzonitrile should be handled with caution. It has the potential to react violently with other chemicals, and appropriate safety measures, such as wearing protective gear and working in a controlled environment, should be taken to minimize risks.

Check Digit Verification of cas no

The CAS Registry Mumber 17823-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,2 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17823-35:
(7*1)+(6*7)+(5*8)+(4*2)+(3*3)+(2*3)+(1*5)=117
117 % 10 = 7
So 17823-35-7 is a valid CAS Registry Number.

17823-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetrafluoro-4-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names Benzonitrile,2,3,5,6-tetrafluoro-4-nitro

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:17823-35-7 SDS

17823-35-7Downstream Products

17823-35-7Relevant academic research and scientific papers

Sequential continuous flow processes for the oxidation of amines and azides by using HOF·MeCN

McPake, Christopher B.,Murray, Christopher B.,Sandford, Graham

experimental part, p. 312 - 319 (2012/06/15)

The generation and use of the highly potent oxidising agent HOF·MeCN in a controlled single continuous flow process is described. Oxidations of amines and azides to corresponding nitrated systems by using fluorine gas, water and acetonitrile by sequential gas-liquid/liquid-liquid continuous flow procedures are reported. Oxidation in flow: The oxidation of amines and azides to the corresponding nitrated systems by using fluorine gas, water and acetonitrile by sequential gas-liquid/liquid-liquid continuous flow procedures are reported. Copyright

RADICAL-ANIONS OF AROMATIC COMPOUNDS. XXI. THE RADICAL-ANIONS OF 4-SUBSTITUTED 2,6-DIFLUORO- AND 2,3,5,6-TETRAFLUORONITROBENZENES

Selivanova, G. A.,Starichenko, V. F.,Ryabinin, V. A.,Shteingarts, V. D.

, p. 1140 - 1147 (2007/10/02)

For the radical-anions of the series of 4-substituted nitrobenzenes it was established that it fluorine atoms are introduced at both ortho positions of the nitro group the sensitivity of the nature of the para substituent is increased for the spin-spin co

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