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2243-73-4

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2243-73-4 Usage

General Description

3-NITROBENZANILIDE is a chemical compound belonging to the class of organic nitro compounds. It is derived from benzoyl chloride and 3-nitroaniline, and is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and agrichemicals. 3-NITROBENZANILIDE is known for its pale yellow crystalline appearance and is sparingly soluble in water. It is important to handle 3-NITROBENZANILIDE with caution as it is considered a hazardous substance and may have toxic effects on human health and the environment if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 2243-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,4 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2243-73:
(6*2)+(5*2)+(4*4)+(3*3)+(2*7)+(1*3)=64
64 % 10 = 4
So 2243-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O3/c16-13(14-11-6-2-1-3-7-11)10-5-4-8-12(9-10)15(17)18/h1-9H,(H,14,16)

2243-73-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H60695)  3-Nitro-N-phenylbenzamide, 97%   

  • 2243-73-4

  • 250mg

  • 1273.0CNY

  • Detail
  • Alfa Aesar

  • (H60695)  3-Nitro-N-phenylbenzamide, 97%   

  • 2243-73-4

  • 1g

  • 4069.0CNY

  • Detail

2243-73-4SDS

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 3-NITROBENZANILIDE

1.2 Other means of identification

Product number -
Other names 3-Nitro-benzoesaeure-anilid

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:2243-73-4 SDS

2243-73-4Relevant articles and documents

Activated charcoal supported copper nanoparticles: A readily available and inexpensive heterogeneous catalyst for the N-arylation of primary amides and lactams with aryl iodides

Zhao, Rong,Dong, Wenwen,Teng, Jiangge,Wang, Zhiwei,Wang, Yunzhong,Yang, Jianguo,Jia, Qiang,Chu, Changhu

supporting information, (2020/12/21)

A novel heterogeneous copper catalyst has been developed by supporting copper nanoparticles on activated charcoal via in situ reducing copper(II) with aqueous hydrazine as reductant. The characterization of Cu/C catalyst showed that the Cu0 nano-particles were formed on the surface of charcoal. This catalyst displayed good catalytic activities toward the N-arylation of primary amides and lactams with aryl iodides.

Method for synthesizing amide compound through photocatalysis in water phase

-

Paragraph 0018-0048, (2019/10/01)

The invention discloses a method for synthesizing an amide compound through photocatalysis in a water phase. The method comprises the following steps: putting catalysis amounts of a free radical initiator, an amine derivative, a carboxylic acid derivative, a phase transfer catalyst, an inorganic base and water into a reaction container, carrying out a reaction in a photocatalysis reaction instrument at certain power under a room temperature condition, after a certain time, carrying out extraction by using a small amount of ethyl acetate, and carrying out recrystallization, so as to obtain theamide compound, wherein the free radical initiator is eosin, methyl orange, sodium persulfate, ammonium persulfate or potassium peroxodisulfate, the phase transfer catalyst is tetrabutylammonium bromide, and the power of the photocatalytic reaction instrument is 5W. By adopting the method disclosed by the invention, toxic thionyl chloride or phosphorus oxychloride is not needed for a chlorinationreaction, water is adopted as a solvent, a novel photocatalysis method is used, and the amide compound with a high yield can be prepared through a room-temperature reaction for 2-5 hours with an incandescent light bulb of 5W, and in addition, the method is simple in aftertreatment, and low in cost and is an ideal green synthesis method of amide compounds.

The visualization of hERG channels in living cells: Via a fluorescent probe regulated by the synergy between solvatochromism and molecular rotation based on simple targeting of the group 4-benzylaniline

Qiao, Zhen,Zhou, Qiqi,Zhang, Hongyi,Wei, Ningning,Zhang, Yanru,Wang, Kewei

supporting information, p. 5515 - 5518 (2019/05/16)

A highly sensitive fluorescent probe CBH based on solvatochromism and molecular rotation was designed and developed for imaging of hERG channels by employing a novel targeting group 4-benzylaniline. More importantly, CBH has the potential for the quantita

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