879486-47-2 Usage
Uses
Used in Organic Synthesis:
[4-(4'-Aminomorpholine-1-carbonyl)phenyl]-boronic acid pinacol ester is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds in organic synthesis. Its ability to react with diols, amines, and other nucleophiles to form stable covalent bonds makes it a crucial component in creating complex molecular structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [4-(4'-Aminomorpholine-1-carbonyl)phenyl]-boronic acid pinacol ester is employed as a key intermediate in the development of pharmaceuticals. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Pharmaceutical Development:
[4-(4'-Aminomorpholine-1-carbonyl)phenyl]-boronic acid pinacol ester is used as a building block in the design and synthesis of new drugs. Its reactivity and structural diversity contribute to the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Research and Development:
This chemical is also utilized in research and development settings, where it serves as a valuable tool for exploring new reaction pathways and understanding the fundamental principles of chemical reactivity.
Used in Chemical Engineering:
In chemical engineering, [4-(4'-Aminomorpholine-1-carbonyl)phenyl]-boronic acid pinacol ester is employed in the design and optimization of chemical processes, particularly those involving the formation of complex molecular structures and the development of new materials with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 879486-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,4,8 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 879486-47:
(8*8)+(7*7)+(6*9)+(5*4)+(4*8)+(3*6)+(2*4)+(1*7)=252
252 % 10 = 2
So 879486-47-2 is a valid CAS Registry Number.
879486-47-2Relevant academic research and scientific papers
SUBSTITUTED BIPHENYL DERIVATIVE
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Page/Page column 117, (2010/11/27)
The present invention relates to a biaryl derivative or a pharmacologically acceptable salt thereof having an excellent collagen-synthesis inhibition activity. A biaryl derivative having a structure represented by the following General Formula (I) or a pharmacologically acceptable salt thereof: wherein R1 represents a C6-C10 aryl group which is substituted with one to three group(s) each independently selected from the group consisting of a group defined by formula R-L-, a di-(C1-C6 alkyl)amino group, a di-(C1-C6 alkyl)aminosulfonyl group, a hydroxyaminocarbonyl group, and a halogen atom, and so on; R represents a C1-C6 alkyl group, and so on; L represents a sulfonyl group, an aminosulfonyl group, or a sulfonylamino group, and so on; R2 represents a hydrogen atom, and so on; A represents a group defined by formula (II), (III), or (IV); R3 represents a C1-C6 alkyl group, and so on; and R4 represents a C1-C6 alkyl group, and so on.
