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"Acetamide, N-(5-fluoro-2-nitrophenyl)-" is a chemical compound with the molecular formula C8H6FN3O3. It is a derivative of acetamide, featuring a 5-fluoro-2-nitrophenyl group attached to the nitrogen atom. Acetamide, N-(5-fluoro-2-nitrophenyl)- is characterized by the presence of a fluorine atom at the 5th position and a nitro group at the 2nd position of the phenyl ring. It is an organic compound that may be used in the synthesis of pharmaceuticals or other chemical products due to its unique structure and reactivity. The compound's properties, such as its solubility, stability, and potential applications, are influenced by the presence of the fluorine and nitro groups, which can affect its electronic properties and reactivity.

345-14-2

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345-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 345-14-2 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 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 345-14:
(5*3)+(4*4)+(3*5)+(2*1)+(1*4)=52
52 % 10 = 2
So 345-14-2 is a valid CAS Registry Number.

345-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-fluoro-2-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-methylcarbonyl 2-nitro-5-fluoroaniline

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:345-14-2 SDS

345-14-2Relevant academic research and scientific papers

Acetamidoarenediazonium Salts: Opportunities for Multiple Arene Functionalization

Schmidt, Bernd,Elizarov, Nelli,Riemer, Nastja,H?lter, Frank

, p. 5826 - 5841 (2015/09/15)

Unlike their ortho counterparts, meta- and para-acetamidoanilines can be converted into the corresponding acetamidoarenediazonium salts. These offer various opportunities for multiple Pd-catalyzed arene functionalization reactions, such as Matsuda-Heck-, Suzuki-Miyaura- or Fujiwara-Moritani couplings. Acetamidoarenediazonium salts, accessible from simple acetamidoanilines, are starting points for multiple Pd-catalyzed arene functionalization reactions.

SUBSTITUTED BENZIMIDAZOLES

-

Page/Page column 36, (2008/12/04)

Disclosed herein are substituted benzimidazole-based proton pump modulators of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.

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