874290-97-8 Usage
Uses
Used in Organic Synthesis:
4-(Morpholinylcarbonylamino)phenylboronic acid, pinacol ester is used as a reagent for the formation of complex organic molecules due to its unique functional groups. It is particularly valuable in the Suzuki-Miyaura coupling reaction, which is a widely used method for creating carbon-carbon bonds in organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(Morpholinylcarbonylamino)phenylboronic acid, pinacol ester is used as a key intermediate in the synthesis of various drug candidates. Its ability to form carbon-carbon bonds makes it a valuable component in the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Research:
4-(Morpholinylcarbonylamino)phenylboronic acid, pinacol ester is utilized in chemical research as a versatile building block for the synthesis of a wide range of organic compounds. Its reactivity and stability make it an ideal candidate for exploring new chemical reactions and developing novel synthetic pathways.
Used in Material Science:
In the field of material science, 4-(Morpholinylcarbonylamino)phenylboronic acid, pinacol ester is employed in the development of new materials with specific properties. Its ability to form stable bonds and its compatibility with various other chemical groups make it a promising candidate for the synthesis of advanced materials with applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 874290-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,2,9 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 874290-97:
(8*8)+(7*7)+(6*4)+(5*2)+(4*9)+(3*0)+(2*9)+(1*7)=208
208 % 10 = 8
So 874290-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H25BN2O4/c1-16(2)17(3,4)24-18(23-16)13-5-7-14(8-6-13)19-15(21)20-9-11-22-12-10-20/h5-8H,9-12H2,1-4H3,(H,19,21)
874290-97-8Relevant articles and documents
Synthesis, Crystal Structure, and DFT Study of a New Derivative of Pyrido[2,3-d]pyrimidine
Deng, Liyuan,Hu, Weiyin,Liao, Wanpeng,Pan, Hongyan,Sun, Hong,Zhou, Zhixu
, p. 2489 - 2496 (2022/01/22)
Abstract: N-{4-[(6-bromopyrido[2,3-d]pyrimidin-4-yl)oxy]phenyl}morpholine-4-carboxamide has been synthesized as a derivative of pyrido[2,3-d]pyrimidine that demonstrates antitumor, antibacterial, anti-inflammatory, and antimicrobial activities. Synthesis of the target compound based on 2-aminonicotinic acid as the starting material has included its esterification, bromination, cyclization, and substitution reactions. Structure of the product is confirmed by 1H and 13C NMR, FT-IR, and single-crystal X-ray diffraction (XRD). The optimized structure, electrostatic potential and frontier molecular orbitals (FMO) of the compound have been approached by DFT calculations. The compound demonstrates antiproliferative activity on A375 cells.
SUBSTITUTED BIPHENYL DERIVATIVE
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Page/Page column 127, (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.
