105337-21-1 Usage
Description
4-[2-(2-NITROPHENOXY)ETHYL]MORPHOLINE is a nitroaromatic compound that features a morpholine ring with a 2-nitrophenyl group and a 2-(2-nitrophenoxy)ethyl substituent. It is a versatile organic compound with applications in various industries, including pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
4-[2-(2-NITROPHENOXY)ETHYL]MORPHOLINE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into drug molecules, potentially enhancing their therapeutic properties and effectiveness.
Used in Agrochemical Industry:
In the agrochemical sector, 4-[2-(2-NITROPHENOXY)ETHYL]MORPHOLINE serves as an essential component in the development of agrochemicals. Its incorporation into these products can improve their performance in protecting crops from pests and diseases.
Used in Organic Compounds Synthesis:
4-[2-(2-NITROPHENOXY)ETHYL]MORPHOLINE is utilized as an intermediate in the manufacture of a wide range of organic compounds. Its presence in these compounds can contribute to their chemical properties and potential applications.
Used in Dye Industry:
4-[2-(2-NITROPHENOXY)ETHYL]MORPHOLINE also finds use in the dye industry, where it is employed in the production of various dyes. Its unique structure can impart specific color characteristics and properties to the dyes, making them suitable for different applications.
Used in Biological Research:
4-[2-(2-NITROPHENOXY)ETHYL]MORPHOLINE has been studied for its potential biological activities, such as antifungal and antimicrobial properties. Researchers are exploring its potential use in developing new treatments for infections and diseases caused by fungi and bacteria.
However, it is crucial to handle 4-[2-(2-NITROPHENOXY)ETHYL]MORPHOLINE with care due to its potential hazardous properties. Proper safety measures should be taken during its synthesis, storage, and use to minimize any risks associated with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 105337-21-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,3 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105337-21:
(8*1)+(7*0)+(6*5)+(5*3)+(4*3)+(3*7)+(2*2)+(1*1)=91
91 % 10 = 1
So 105337-21-1 is a valid CAS Registry Number.
105337-21-1Relevant articles and documents
Synthesis and p38 inhibitory activity of some novel substituted N,N′-diarylurea derivatives
Zhu, Dianxi,Xing, Qifeng,Cao, Ruiyuan,Zhao, Dongmei,Zhong, Wu
, (2016/07/06)
We have identified a novel series of substituted N,N′-diarylurea p38α inhibitors. The inhibitory activity of the target compounds against the enzyme p38α, MAPKAPK2 in BHK cells, TNF-α release in LPS-stimulated THP-1 cells and p38α binding experiments were
CATIONIC NAPHTHYLDIAZO DYES AND AGENTS CONTAINING SAID DYES USED TO COLOUR KERATIN FIBRES
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Page/Page column 24, (2010/02/14)
The invention relates to cationic naphthyldiazo dyes of general formula (I), and colouring agents containing said dyes, for colouring keratin fibres.
