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1-(4-Morpholino-3-nitrophenyl)-1-ethanone, also known as MNE, is a chemical compound characterized by its molecular formula C10H11NO4. It features a nitrophenyl-containing ketone structure with a morpholine group attached to the aromatic ring. MNE is recognized for its versatility as a building block in the synthesis of pharmaceuticals, agrochemicals, and functional materials, as well as its role as a precursor in the production of dyes and organic compounds. Its unique structural features and reactivity make it a promising candidate in medicinal chemistry and material science, although its potential health and environmental hazards necessitate careful handling.

144783-46-0

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144783-46-0 Usage

Uses

Used in Pharmaceutical Synthesis:
1-(4-Morpholino-3-nitrophenyl)-1-ethanone is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with improved therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 1-(4-Morpholino-3-nitrophenyl)-1-ethanone is utilized as a precursor in the creation of agrochemicals, potentially enhancing crop protection and yield.
Used in Material Science:
1-(4-Morpholino-3-nitrophenyl)-1-ethanone is employed as a component in the development of functional materials, leveraging its structural and reactive characteristics to produce materials with specific properties for various applications.
Used in Dye and Organic Compound Production:
MNE serves as a precursor in the production of certain dyes and organic compounds, contributing to the coloration and functional attributes of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 144783-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,8 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 144783-46:
(8*1)+(7*4)+(6*4)+(5*7)+(4*8)+(3*3)+(2*4)+(1*6)=150
150 % 10 = 0
So 144783-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O4/c1-9(15)10-2-3-11(12(8-10)14(16)17)13-4-6-18-7-5-13/h2-3,8H,4-7H2,1H3

144783-46-0SDS

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 1-(4-morpholin-4-yl-3-nitrophenyl)ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-[4-(4-morpholinyl)-3-nitrophenyl]

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:144783-46-0 SDS

144783-46-0Downstream Products

144783-46-0Relevant academic research and scientific papers

Design, synthesis and biological evaluation of novel aryl-acrylic derivatives as novel indoleamine-2,3-dioxygenase 1 (IDO1) inhibitors

Hu, Hao,Li, Ming,Wu, Di,Li, Zhiwei,Miao, Ruifeng,Liu, Yajing,Gong, Ping

, p. 3135 - 3144 (2019)

Two series of novel aryl-acrylic derivatives were designed, synthesized, and screened in enzymatic and cellular inhibitory activities. All compounds showed moderate to significant potency. The SAR analyses indicated that the semicarbazone linker is better

HETEROCYCLES USEFUL AS IDO AND TDO INHIBITORS

-

Paragraph 125, (2016/10/31)

Provided are compounds of Formula (I) shown below using for treatment of diseases or disorders mediated by IDO and/or TDO, pharmaceutical compositions and methods of preparation thereof.

Synthesis of &β-amino substituted 4-amino-3-nitropropiophenones as diethylcarbamazine analogs and their antifilarial activity

Varma, Rajendra S,Sarin, Simi,Chatterjee, R K

, p. 711 - 713 (2007/10/02)

A number of β-amino substituted 4-amino-3-nitropropiophenones (5-16) have been synthesised and evaluated against filariasis.Compounds 14,10 and 13 show 77.5percent, 74.4percent and 82.2percent microfilaricidal activity respectively, at 30 mg/kg for 5 days by i.p. route.Compound 14 also show 60.3percent adulticidal activity.

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