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N-(2,4-dichloro-5-fluorophenyl)acetamide is a chemical compound with the molecular formula C8H6Cl2FNO. It is an amide derivative, characterized by the presence of an amide functional group (-CONH2) attached to a 2,4-dichloro-5-fluorophenyl ring. Ν-(2,4-dichloro-5-fluorophenyl)acetamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as the presence of halogenated aromatic rings can contribute to the compound's biological activity. The specific combination of chlorine and fluorine atoms in the phenyl ring may influence its reactivity and stability, making it a subject of interest in chemical research and development.

398-92-5

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398-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 398-92-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 398-92:
(5*3)+(4*9)+(3*8)+(2*9)+(1*2)=95
95 % 10 = 5
So 398-92-5 is a valid CAS Registry Number.

398-92-5SDS

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 acetic acid-(2,4-dichloro-5-fluoro-anilide)

1.2 Other means of identification

Product number -
Other names 2.4-Dichlor-5-fluor-N-acetyl-anilin

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:398-92-5 SDS

398-92-5Downstream Products

398-92-5Relevant academic research and scientific papers

A kind of benzo heterocyclic compound and its use for the treatment of cancer (by machine translation)

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Paragraph 0060; 0061; 0062; 0063, (2019/01/14)

The invention of the formula I indicated by the benzo heterocyclic compound, or its pharmaceutically acceptable salt, or its crystalline form, or solvate thereof, or its isotope body, or a tautomer thereof, or stereochemical isomers thereof. The experimen

Solvent-free aromatic C-H functionalisation/halogenation reactions

Bedford, Robin B.,Engelhart, Jens U.,Haddow, Mairi F.,Mitchell, Charlotte J.,Webster, Ruth L.

supporting information; experimental part, p. 10464 - 10472 (2011/01/05)

The solvent-free, palladium-catalysed reaction of anilides with CuCl 2 in the presence or absence of copper acetate yields ortho-chlorinated anilides in good to excellent yields, even on a large scale (100 mmol). By contrast, the equivalent reactions with copper bromide, either solvent free or in 1,2-dichloroethane, in the presence or absence of palladium, under air or inert conditions, gave the products of simple electrophilic bromination. Mechanistic studies highlighted the involvement of palladacyclic intermediates, one of which was characterised crystallographically, which undergo subsequent reaction with copper(ii) chloride to yield the chlorinated anilide products.

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