1163721-90-1 Usage
Description
(Z)-3-Dimethylamino-1-(3-nitro-phenyl)-propenone, also known as 3-Dimethylamino-1-(3-nitrophenyl)prop-2-en-1-one, is a chemical compound with the molecular formula C11H12N2O3. It is a yellow to brown crystalline powder with a molecular weight of 220.22 g/mol. (Z)-3-Dimethylamino-1-(3-nitro-phenyl)-propenone is a derivative of benzaldehyde and is known for its potential use as a precursor in the preparation of pharmaceuticals and agrochemicals. It is also recognized for its potential biological and pharmacological activities, making it a subject of interest in the field of medicinal chemistry. However, due to its potential hazardous nature, proper care and precautions are required in handling and using this compound.
Uses
Used in Pharmaceutical Industry:
(Z)-3-Dimethylamino-1-(3-nitro-phenyl)-propenone is used as a precursor for the synthesis of various pharmaceuticals due to its unique chemical structure and potential biological activities. Its role in the creation of new drugs is significant, as it can contribute to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, (Z)-3-Dimethylamino-1-(3-nitro-phenyl)-propenone is used as a starting material for the development of new agrochemicals. Its potential use in this field is attributed to its ability to be synthesized into various organic compounds that can be utilized in the production of pesticides, herbicides, and other agricultural products.
Used in Medicinal Chemistry Research:
(Z)-3-Dimethylamino-1-(3-nitro-phenyl)-propenone is also used as a subject of interest in medicinal chemistry research. Its potential biological and pharmacological activities make it a valuable compound for studying and understanding various biological processes and the development of new drugs to target specific medical conditions.
Safety Precautions:
Due to the potential hazardous nature of (Z)-3-Dimethylamino-1-(3-nitro-phenyl)-propenone, it is crucial to follow proper safety protocols when handling and using this compound. This includes wearing appropriate personal protective equipment (PPE), working in a well-ventilated area, and following established guidelines for the safe handling and disposal of hazardous chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1163721-90-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,3,7,2 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1163721-90:
(9*1)+(8*1)+(7*6)+(6*3)+(5*7)+(4*2)+(3*1)+(2*9)+(1*0)=141
141 % 10 = 1
So 1163721-90-1 is a valid CAS Registry Number.
1163721-90-1Relevant articles and documents
Design, synthesis, in silico, and in vitro evaluation of 3-phenylpyrazole acetamide derivatives as antimycobacterial agents
Gaikwad, Nikhil B.,Nirmale, Krishna,Sahoo, Santosh K.,Ahmad, Mohammad N.,Kaul, Grace,Shukla, Manjulika,Nanduri, Srinivas,Das Gupta, Arunava,Chopra, Sidharth,Yaddanapudi, Madhavi V.
, (2020/12/23)
Mycobacterium tuberculosis (Mtb) is one of the most dangerous pathogens affecting immunocompetent and immunocompromised patients worldwide. Novel molecules, which are efficient and can reduce the duration of therapy against drug-resistant strains, are an
COMPOUND OF 5-HYDROXYL-1,7-NAPHTHYRIDINE SUBSTITUTED BY ARYL OR HETEROARYL, PREPARATION METHOD THEREOF AND PHARMACEUTICAL USE THEREOF
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Paragraph 0154, (2018/03/25)
Disclosed are a compound of the following formula (I) or a pharmaceutically acceptable salt thereof, a preparation method thereof, pharmaceutical compositions and uses thereof in the preparation of a medicine for inhibiting HIF prolyl hydroxylase or a medicine for promoting the generation of endogenous EPO, wherein in the formula (I), R1 and R2 are each independently hydrogen; R3 is hydrogen or C1-3 alkyl; and Ar is an aromatic ring or an heteroaromatic ring selected from a naphthalene ring, a pyridine ring, a thiophene ring, a furan ring and a substituted benzene ring.
Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond Functionalization
Liang, Gaohui,Rong, Jiaxin,Sun, Wangbin,Chen, Gengjia,Jiang, Yaojia,Loh, Teck-Peng
supporting information, p. 7326 - 7331 (2018/11/25)
An expedient [5 + 1] annulation method via Rh(III)-catalyzed C-H bond functionalization of enaminones to synthesize polyaromatic rings is described. The reaction tolerates a broad range of functional groups and offers a new entry to construct polycyclic a
