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4-Methylsulfanylbenzamide oxime, with the molecular formula C8H9N3OS, is an oxime derivative of 4-methylsulfanylbenzamide. It is a chemical compound that serves as a reagent in organic synthesis and has potential applications in pharmaceuticals, agrochemicals, and as an anti-cancer agent. Its unique properties and potential uses make it a subject of interest in various research and development fields.

500024-30-6

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500024-30-6 Usage

Uses

Used in Organic Synthesis:
4-Methylsulfanylbenzamide oxime is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methylsulfanylbenzamide oxime is used as a precursor in the development of new drugs, leveraging its chemical properties to create novel therapeutic agents.
Used in Agrochemical Industry:
4-Methylsulfanylbenzamide oxime is utilized in the agrochemical industry as a component in the synthesis of pesticides and other agricultural chemicals, aiming to enhance crop protection and yield.
Used in Anti-Cancer Research:
4-Methylsulfanylbenzamide oxime is studied as a potential anti-cancer agent, with research focusing on its ability to target and inhibit the growth of cancer cells, offering a new avenue for cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 500024-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,0,2 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 500024-30:
(8*5)+(7*0)+(6*0)+(5*0)+(4*2)+(3*4)+(2*3)+(1*0)=66
66 % 10 = 6
So 500024-30-6 is a valid CAS Registry Number.

500024-30-6SDS

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 N'-hydroxy-4-methylsulfanylbenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names N-hydroxy-4-methylsulfanylbenzamidine

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:500024-30-6 SDS

500024-30-6Relevant academic research and scientific papers

Imidazole hydrochloride promoted synthesis of 3,5-disubstituted-1,2,4-oxadiazoles

Wang, Xuetong,Wang, Yin,Liu, Xiaoling,He, Tingshu,Li, Lingli,Wu, Huili,Zhou, Shangjun,Li, Dan,Liao, Siwei,Xu, Ping,Huang, Xing,Yuan, Jianyong

supporting information, (2021/10/14)

Imidazole hydrochloride as an additive promotes the reaction of amidoximes and DMA derivatives to generated 3,5-disubstituted-1,2,4-oxadiazoles in low to excellent yields without the use of coupling reagents, oxidants, strong acids or bases and other additives.

Synthesis of Some Azamacrocycles Bearing 1,2,4-Oxadiazole and 1,2,3-Triazole Moieties

?zer, B.,Dürüst, Y.

, p. 698 - 705 (2020/06/01)

Abstract: A tetraazacrown ether,4,9-di(prop-2-yn-1-yl)-1,4,9,12-tetraazacyclohexadecane-2,11-dione, bearingpropargyl groups on two nitrogens was synthesized starting from1,4,9,12-tetraazacyclohexadecane-2,11-dione and subjected to 1,3-cycloadditionreactio

FUNGICIDAL OXADIAZOLES

-

Page/Page column 62, (2018/05/24)

Disclosed are compounds of Formula I, including all geometric and stereoisomers, tautomers, N-oxides, and salts thereof, wherein R1, Z1, R2, Z2, J, s and f are as defined in the disclosure. Also disclosed are co

An Efficient Synthesis of 2-Substituted Quinazolin-4(3 H)-ones Catalyzed by Iron(III) Chloride

Mekala, Ramamohan,Akula, Raghunadh,Kamaraju, Raghavendra Rao,Bannoth, Chandrasekhar Kothapalli,Regati, Sridhar,Sarva, Jayaprakash

supporting information, p. 821 - 826 (2014/04/03)

A simple and highly efficient synthesis of 2-substituted quinazolin-4(3H)-ones by the iron(III) chloride catalyzed reaction of isatoic anhydride with various amidoxime derivatives was developed. Several aryl and alkyl amidoximes were screened to demonstra

Synthesis and anti-protozoal activity of novel dihydropyrrolo[3,4-d][1,2,3] triazoles

Dürüst, Yaar,Karaku, Hamza,Kaiser, Marcel,Tasdemir, Deniz

scheme or table, p. 296 - 304 (2012/03/27)

1,2,4-Oxadiazole and 1,2,3-triazole containing heterocyclic compounds continue to gain interest in synthesis of chemical entities and exhibit various biological activities as anti-protozoal and anti-cancer agents. By using the principle of bioisosterism,

HETEROARYL SUBSTITUTED PYRAZOLE DERIVATIVES USEFUL FOR TREATING HYPER-PROLIFERATIVE DISORDERS AND DISEASES ASSOCIATED WITH ANGIOGENESIS

-

Page/Page column 91, (2009/01/20)

This invention relates to novel heteroaryl substituted pyrazole compounds, pharmaceutical compositions containing such compounds and the use of those compounds or compositions for treating hyper-proliferative and/or angiogenesis disorders, as a sole agent or in combination with other active ingredients or therapeutic measures.

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