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23610-05-1

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23610-05-1 Usage

General Description

4-[(Z)-Amino(hydroxyimino)methyl]benzoic acid, also known as Z-AHMB, is a chemical compound that belongs to the class of benzoic acids. It contains an amino group, a hydroxyimino group, and a carboxylic acid group attached to a benzene ring. Z-AHMB has potential pharmaceutical applications due to its ability to act as an antioxidant and anti-inflammatory agent. It has also been studied for its potential use in the treatment of various diseases and conditions such as cancer, inflammation, and oxidative stress. Z-AHMB is a promising chemical compound that may have therapeutic benefits in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 23610-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,1 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23610-05:
(7*2)+(6*3)+(5*6)+(4*1)+(3*0)+(2*0)+(1*5)=71
71 % 10 = 1
So 23610-05-1 is a valid CAS Registry Number.

23610-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(N-hydroxycarbamimidoyl)-benzoic acid

1.2 Other means of identification

Product number -
Other names Benzenylamidoxim-p-carbonsaeure

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:23610-05-1 SDS

23610-05-1Relevant articles and documents

Synthesis, Antifungal Activity, DFT Study and Molecular Dynamics Simulation of Novel 4-(1,2,4-Oxadiazol-3-yl)-N-(4-phenoxyphenyl)benzamide Derivatives

Yang, Zihui,Liu, Qingsong,Sun, Yue,Sun, Xuebao,Chen, Linlin,Sun, Lu,Gu, Wen

, (2021/11/10)

In order to find novel potential antifungal agrochemicals, a series of new 4-(1,2,4-oxadiazol-3-yl)-N-(4-phenoxyphenyl)benzamide derivatives 3a–j were designed, synthesized and characterized by their 1H-, 13C-NMR and HRMS spectra. Th

Development of Potent 3-Br-isoxazoline-Based Antimalarial and Antileishmanial Compounds

Basilico, Nicoletta,Conti, Paola,Coser, Consuelo,Galbiati, Andrea,Parapini, Silvia,Tamborini, Lucia,Taramelli, Donatella,Zana, Aureliano

supporting information, p. 1726 - 1732 (2021/11/01)

Starting from the structure of previously reported 3-Br-isoxazoline-based covalent inhibitors of P. falciparum glyceraldehyde 3-phosphate dehydrogenase, and with the intent to improve their metabolic stability and antimalarial activity, we designed and synthesized a series of simplified analogues that are characterized by the insertion of the oxadiazole ring as a bioisosteric replacement for the metabolically labile ester/amide function. We then further replaced the oxadiazole ring with a series of five-membered heterocycles and finally combined the most promising structural features. All the new derivatives were tested in vitro for antimalarial as well as antileishmanial activity. We identified two very promising new lead compounds, endowed with submicromolar antileishmanial activity and nanomolar antiplasmodial activity, respectively, and a very high selectivity index with respect to mammalian cells.

SUBSTITUTED TRIFLUOROMETHYLOXADIAZOLES FOR COMBATING PHYTOPATHOGENIC FUNGI

-

Paragraph 68, (2019/03/14)

The present invention relates to trifluoromethyloxadiazoles of the formula I, or the N-oxides, or the agriculturally useful salts thereof, and the use thereof for controlling phytopathogenic fungi; to a method for combating phytopathogenic harmful fungi,

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