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866579-96-6

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866579-96-6 Usage

General Description

2'-Fluoro-4'-nitroacetophenone is a chemical compound with the molecular formula C8H6FNO3. It is a yellow solid with a molecular weight of 181.13 g/mol. 2'-Fluoro-4'-nitroacetophenone is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. 2'-Fluoro-4'-nitroacetophenone is commonly used in research and development, particularly in the pharmaceutical industry, due to its versatile chemical properties and potential applications. It is important to handle this compound with caution, as it may be hazardous if not properly handled and stored.

Check Digit Verification of cas no

The CAS Registry Mumber 866579-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,5,7 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 866579-96:
(8*8)+(7*6)+(6*6)+(5*5)+(4*7)+(3*9)+(2*9)+(1*6)=246
246 % 10 = 6
So 866579-96-6 is a valid CAS Registry Number.

866579-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-fluoro-4-nitrophenyl)ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-(2-fluoro-4-nitrophenyl)-

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:866579-96-6 SDS

866579-96-6Relevant articles and documents

Synthesis of 2-fluorocholine aryl carbonyl compounds

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Paragraph 0068; 0069; 0072, (2017/02/09)

The invention provides a method for synthesizing 2-fluoroarylcarbonyl compounds, which comprises the following steps: converting arylcarbonyl compounds into corresponding carbonyl oxime ether compounds, mildly implementing aryl hydrocarbon chain direct fluoridation of high-selectivity oximido substituent group ortho-position in the presence of a palladium catalyst, a fluoridation reagent and additives, and finally, rehydrolyzing oxime ethers under the action of acid to obtain the 2-fluoroarylcarbonyl compounds. The fluoridation method has the advantages of mild reaction conditions, high substrate adaptability, high fluoridation selectivity and the like, is simple to operate, and has higher application research value.

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