26162-89-0 Usage
Uses
Used in Pharmaceutical and Medicinal Chemistry:
Morpholino(2-nitrophenyl)methanone is used as a building block for the synthesis of various pharmaceuticals and biologically active molecules, leveraging its unique structural features to enhance the properties and efficacy of these compounds.
Used in Anti-inflammatory Applications:
Morpholino(2-nitrophenyl)methanone is utilized as an anti-inflammatory agent, potentially mitigating inflammation through its interaction with biological systems and contributing to the management of inflammatory conditions.
Used in Anticancer Applications:
As an anticancer agent, morpholino(2-nitrophenyl)methanone may exhibit properties that help in the treatment of cancer by interfering with cancer cell growth and proliferation, offering a potential therapeutic approach in oncology.
Used in Materials Science:
In the field of materials science, morpholino(2-nitrophenyl)methanone is applied in the development of new polymers and polymer blends. Its incorporation can lead to materials with specialized properties, such as improved mechanical strength, thermal stability, or specific interactions with other molecules, broadening its utility in various industries.
Used in Organic Synthesis:
Morpholino(2-nitrophenyl)methanone is employed as a key intermediate in organic synthesis, where it can be used to construct complex organic molecules, contributing to the advancement of chemical research and the development of novel chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 26162-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26162-89:
(7*2)+(6*6)+(5*1)+(4*6)+(3*2)+(2*8)+(1*9)=110
110 % 10 = 0
So 26162-89-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O4/c14-11(12-5-7-17-8-6-12)9-3-1-2-4-10(9)13(15)16/h1-4H,5-8H2
26162-89-0Relevant academic research and scientific papers
Co2(CO)8 as a convenient in situ CO source for the direct synthesis of benzamides from aryl halides (Br/I) via aminocarbonylation
Baburajan, Poongavanam,Elango, Kuppanagounder P.
supporting information, p. 1006 - 1010 (2014/02/14)
A fast, mild, and functional group tolerant method for the direct synthesis of benzamides from aryl halides (Br, I) via aminocarbonylation, using solid Co2(CO)8 as a convenient CO source, has been demonstrated. The developed method is applicable to a wide variety of 1 and cyclic and acyclic 2 amines. Nitro substituted (o, m and p) aryl halides have easily been converted to the corresponding benzamides, without the reduction of the nitro group, in high yields using this in situ carbonylation methodology under microwave irradiation.
Co2(CO)8 as a convenient in situ CO source for the direct synthesis of benzamides from aryl halides (Br/I) via aminocarbonylation
Baburajan, Poongavanam,Elango, Kuppanagounder P.
supporting information, p. 1006 - 1010 (2015/02/19)
A fast, mild, and functional group tolerant method for the direct synthesis of benzamides from aryl halides (Br, I) via aminocarbonylation, using solid Co2(CO)8 as a convenient CO source, has been demonstrated. The developed method is applicable to a wide variety of 1° and cyclic and acyclic 2°amines. Nitro substituted (o, m and p) aryl halides have easily been converted to the corresponding benzamides, without the reduction of the nitro group, in high yields using this in situ carbonylation methodology under microwave irradiation.
