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1,3-bis(3-morpholinopropyl)urea, also known as MorD, is a chemical compound with the molecular formula C15H30N4O4. It is a bis-urea derivative, featuring two morpholinopropyl groups attached to a central urea moiety. MorD is known for its potential applications in various fields, including pharmaceuticals and materials science. It has been studied for its ability to inhibit the enzyme carbonic anhydrase, which plays a role in various physiological processes and diseases. The compound's structure allows it to form hydrogen bonds with the active site of the enzyme, thereby blocking its activity. This property makes MorD a candidate for the development of drugs targeting conditions related to carbonic anhydrase dysregulation. Additionally, its unique structure and properties may also be explored for other applications, such as in the creation of new materials or as a chemical intermediate in the synthesis of other compounds.

6543-79-9

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6543-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6543-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6543-79:
(6*6)+(5*5)+(4*4)+(3*3)+(2*7)+(1*9)=109
109 % 10 = 9
So 6543-79-9 is a valid CAS Registry Number.

6543-79-9Downstream Products

6543-79-9Relevant academic research and scientific papers

Selective N-methylation of aliphatic amines with CO2 and hydrosilanes using nickel-phosphine catalysts

Gonzlez-Sebastin, Lucero,Flores-Alamo, Marcos,Garca, Juventino J.

, p. 763 - 769 (2015/05/12)

A method using CO2 and PhSiH3 for the methylation of primary and secondary aliphatic amines catalyzed by Ni (0) complexes was developed, selectively producing the monomethylated products in moderate to good yields. For that purpose, two catalysts were used: [(dippe)Ni(μ-H)]2 and the commercially available Ni(COD)2/dcype, both of which were rather efficient in this process. With a slight experimental modification, the reaction allowed the production of monomethylated ureas in good yields by using low amounts of PhSiH3. On the basis of the experimental results, we propose a possible reaction mechanism for the formation of the new C-N bond.

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