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1897-53-6

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1897-53-6 Usage

General Description

2-Fluoroterephthalonitrile is a chemical compound with the molecular formula C8H3FNO2. It is a white crystalline solid with a molecular weight of 165.1 g/mol. 2-Fluoroterephthalonitrile is primarily used as an intermediate in the production of pharmaceuticals, agrochemicals, dyes, and pigments. It is also used in the manufacturing of polymers and as a building block in organic synthesis. The compound is considered to be moderately hazardous, with potential health effects including skin and eye irritation, respiratory irritation, and central nervous system effects. It is important to handle 2-Fluoroterephthalonitrile with care and follow proper safety precautions when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1897-53-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,9 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1897-53:
(6*1)+(5*8)+(4*9)+(3*7)+(2*5)+(1*3)=116
116 % 10 = 6
So 1897-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H3FN2/c9-8-3-6(4-10)1-2-7(8)5-11/h1-3H

1897-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluorobenzene-1,4-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 2-Fluoro-1,4-benzenedicarbonitrile

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:1897-53-6 SDS

1897-53-6Relevant articles and documents

Preparation method of aromatic dicarboxylic acid derivative

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Paragraph 0025; 0041-0044, (2021/03/11)

The invention provides a preparation method of an aromatic dicarboxylic acid derivative, wherein the preparation method comprises the following steps: step 1, carrying out a coupling reaction on dihalogenated aromatic hydrocarbon and metal cyanide at a temperature of 40-200 DEG C under metal catalysis in a solvent, and carrying out extraction layering concentration to obtain a dicyano compound after the reaction is finished; and step 2, carrying out a hydrolysis reaction on the obtained dicyanogen compound at the temperature of 60-200 DEG C under an acidic condition, and carrying out post-treatment to obtain the final product. According to the preparation method of the aromatic dicarboxylic acid derivative, dihalogenated aromatic hydrocarbon reacts with metal cyanide and then is hydrolyzedunder the acidic condition to obtain aromatic acid or the derivative thereof, and the preparation method has the remarkable advantages that the raw materials are cheap and easy to obtain, operation is easy and convenient, the yield is high, three wastes are easy to dispose, the product quality is high, and the substrate tolerance is good.

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENTS, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE

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Paragraph 0364; 0365, (2016/06/06)

A compound is represented by a formula (1) below, in which k is an integer of 0 or more, m is an integer of 1 or more, n is an integer of 2 or more. L is a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 30 ring carbon atoms, CN is a cyano group, and D1 and D2 are each independently represented by one of a formula (2), a formula (3) and formula (3x) below, D1 and D2 being optionally mutually the same or different.

ANTIPARASITIC AGENTS

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, (2008/12/07)

The present invention relates to compounds of the formula (I) or a tautomer or prodrug thereof, or a pharmaceutically acceptable salt of said compound, tautomer or prodrug, wherein: R1, R2, R3, R4 and R5 are each independently selected from H, halo, CN, CF3 and CONH2; compositions containing such compounds and the uses of such compounds as antiparasitic agents.

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