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Benzamide, N-(2-aminophenyl)-4-nitro-, also known as 4-Nitro-N-(2-aminophenyl)benzamide, is a chemical compound with the molecular formula C13H11N3O3. It is a derivative of benzamide, featuring a nitro group at the 4-position and an amino group at the 2-position of the phenyl ring. Benzamide, N-(2-aminophenyl)-4-nitro- is often used in the synthesis of pharmaceuticals and other organic compounds due to its versatile chemical structure. It is typically obtained through chemical reactions involving benzoic acid derivatives and aniline, followed by nitration. The compound is known for its potential applications in the development of drugs targeting various therapeutic areas, such as anti-inflammatory and analgesic medications.

6338-73-4

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6338-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6338-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6338-73:
(6*6)+(5*3)+(4*3)+(3*8)+(2*7)+(1*3)=104
104 % 10 = 4
So 6338-73-4 is a valid CAS Registry Number.

6338-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-aminophenyl)-4-nitrobenzamide

1.2 Other means of identification

Product number -
Other names N-(p-Nitrobenzoyl)-o-phenylendiamin

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:6338-73-4 SDS

6338-73-4Relevant academic research and scientific papers

Copper-catalyzed regioselective 2-amination of o-haloanilides with aqueous ammonia

Tang, Yan-Ling,Li, Mei-Ling,Gao, Jin-Chun,Sun, Yun,Qu, Lu,Huang, Feng,Mao, Ze-Wei

supporting information, (2021/04/02)

An efficient Cu(II)-vasicine catalytic system has been developed for intramolecular C[sbnd]N bond formation. In this way, regioselective 2-amination of o-haloanilides with aqueous ammonia in EtOH has been achieved. This strategy provides several advantages, such as good regioselectivity, high yields and functional group tolerance.

Azobenzene-diamides as Photopharmacological Ligands for Insect Ryanodine Receptor

Chen, Meijun,Li, Yuxin,Shao, Xusheng,Wang, Long,Xia, Shanshan,Xu, Zhiping

, p. 14409 - 14416 (2020/12/22)

Photoresponsive ligands are powerful tool compounds for studying receptor function with spatiotemporal resolution. However, to the best of our knowledge, such a ligand is not available for the ryanodine receptor (RyR). Herein, we present a photochromic ligand (PCL) for insect RyR by decorating chlorantraniliprole (CHL) with photoswitchable azobenzene (AB). We demonstrated that one potent ligand, named ABCHL13, shows light-induced reversible trans-cis isomerization and 3.5-fold insecticidal activity decrease toward oriental armyworm (Mythimna separata) after UV-light irradiation, that is, trans-ABCH13 has higher activity than the cis-ABCH13. ABCHL13 enables optical control over intracellular Ca2+ release in dorsal unpaired median (DUM) neurons of M. separata and American cockroach (Periplaneta americana) and cardiac function of P. americana. Our results provide a first photopharmacological toolkit that is applicable to light-dependent regulation of RyR and heart beating.

ANTIMICROBIAL COMPOUNDS

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Page/Page column 33; 34, (2015/05/19)

The invention provides compounds for use in treating microbial infection in an animal. Example compounds include Pyridin-3-ylmethyl (4-((2-aminophenyl)- carbamoyl)benzyl)carbamate ("Entinostat"). The compounds can act via induction of the innate antimicrobial peptide defense system, and stimulation of autophagy.

Zeolites. Efficient and eco-friendly catalysts for the synthesis of benzimidazoles

Heravi, Majid M.,Tajbakhsh, Mahmood,Ahmadi, Amir N.,Mohajerani, Bagher

, p. 175 - 179 (2007/10/03)

A superior method of synthesis of 2-substituted benzimidazoles by means of the heterogeneous catalysis of synthetic and natural zeolites in the reaction of 1,2-diaminobenzene with acid chlorides is described. Springer-Verlag 2005.

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