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C-[3-(2-CHLORO-PHENYL)-ISOXAZOL-5-YL]-METHYLAMINE is a chemical compound that belongs to the class of isoxazole derivatives. It features a methylamine group attached to an isoxazol ring with a 2-chloro-phenyl substituent. C-[3-(2-CHLORO-PHENYL)-ISOXAZOL-5-YL]-METHYLAMINE is of interest in medicinal chemistry, particularly for the development of pharmaceuticals and agrochemicals due to the biological activities exhibited by the isoxazole ring and the potential enhancement of activity provided by the 2-chloro-phenyl group.

543713-32-2

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543713-32-2 Usage

Uses

Used in Pharmaceutical Development:
C-[3-(2-CHLORO-PHENYL)-ISOXAZOL-5-YL]-METHYLAMINE is used as a building block in the synthesis of pharmaceuticals for its potential biological activity. The isoxazole ring is a valuable structural motif in drug discovery, and the presence of the 2-chloro-phenyl group may further enhance its effectiveness in various therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, C-[3-(2-CHLORO-PHENYL)-ISOXAZOL-5-YL]-METHYLAMINE is used as a precursor in the development of agrochemicals. Its unique structure and potential biological activity make it a candidate for creating new compounds that can be used in agriculture for pest control and crop protection.
Further research and studies in the field of organic chemistry and drug development are necessary to fully understand the specific properties and potential applications of C-[3-(2-CHLORO-PHENYL)-ISOXAZOL-5-YL]-METHYLAMINE.

Check Digit Verification of cas no

The CAS Registry Mumber 543713-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,3,7,1 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 543713-32:
(8*5)+(7*4)+(6*3)+(5*7)+(4*1)+(3*3)+(2*3)+(1*2)=142
142 % 10 = 2
So 543713-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClN2O/c11-9-4-2-1-3-8(9)10-5-7(6-12)14-13-10/h1-5H,6,12H2

543713-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(2-chlorophenyl)-1,2-oxazol-5-yl]methanamine

1.2 Other means of identification

Product number -
Other names 3-o-chlorophenyl-5-aminomethyl-isoxazole

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:543713-32-2 SDS

543713-32-2Relevant academic research and scientific papers

Synthesis and preliminary antibacterial evaluation of 2-butyl succinate-based hydroxamate derivatives containing isoxazole rings

Zhang, Datong,Jia, Jiong,Meng, Lijuan,Xu, Weiren,Tang, Lida,Wang, Jianwu

, p. 831 - 842 (2012/01/04)

Two series of novel 2-butyl succinate-based Hydroxamate derivatives containing isoxazole rings were synthesized, characterized and evaluated for antibacterial activity. The synthesized compounds were found to exhibit weak to moderate inhibitory activity against Staphytlococcus aureu and Klebsiellar pneumonia in vitro. All the compounds synthesized were found to be more effective against Klebsiellar pneumonia compared to Staphytlococcus aureu.

Design, synthesis, and herbicidal activities of novel 2-cyanoacrylates containing isoxazole moieties

Liu, Yuxiu,Cui, Zhipeng,Liu, Bin,Cai, Baoli,Li, Yonghong,Wang, Qingmin

, p. 2685 - 2689 (2011/07/07)

A series of novel 2-cyanoacrylates containing an isoxazole moiety were designed and synthesized. Their structures were characterized by 1H NMR and elemental analysis (or high-resolution mass spectrometry). Their herbicidal activities against four species were evaluated, and the results indicated that some of the title compounds showed excellent herbicidal activities against rape and amaranth pigweed in postemergence treatment even at a dose of 75 g/ha.

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