46133-07-7 Usage
Description
(E)-benzene-1,3-diylbis(N-hydroxymethanimine) is an organic chemical compound with the molecular formula C14H14N2O2. It consists of a benzene ring with two N-hydroxymethanimine groups attached in a para position, which allows it to act as a bidentate ligand. (E)-benzene-1,3-diylbis(N-hydroxymethanimine) is known for its versatility in various applications across different industries.
Uses
Used in Coordination Compounds and Metal Complexes:
(E)-benzene-1,3-diylbis(N-hydroxymethanimine) is used as a bidentate ligand for the preparation of coordination compounds and metal complexes. Its ability to chelate with metal ions makes it a valuable component in the synthesis of these complexes, which have applications in various fields, including catalysis, materials science, and bioinorganic chemistry.
Used in Organic Dyes and Pigments:
(E)-benzene-1,3-diylbis(N-hydroxymethanimine) is also utilized in the synthesis of organic dyes and pigments. Its chemical structure contributes to the color properties of the dyes, making it a useful building block for creating a wide range of colors in the dye and pigment industry.
Used in Medicinal Chemistry:
(E)-benzene-1,3-diylbis(N-hydroxymethanimine) has potential applications in the field of medicinal chemistry. Its unique structure and properties make it a promising candidate for the development of new drugs and pharmaceuticals, particularly in the design of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 46133-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,1,3 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 46133-07:
(7*4)+(6*6)+(5*1)+(4*3)+(3*3)+(2*0)+(1*7)=97
97 % 10 = 7
So 46133-07-7 is a valid CAS Registry Number.
46133-07-7Relevant articles and documents
BSA nanoparticles as controlled release carriers for isophethalaldoxime palladacycle complex; Synthesis, characterization,: In vitro evaluation, cytotoxicity and release kinetics analysis
Amirghofran, Zahra,Hajiaghasi, Afsaneh,Jamshidian, Nasrin,Karami, Kazem
, p. 4394 - 4405 (2020)
A new oxime ligand named isophthalaldoxime (1) was synthesized by the addition of hydroxylamine hydrochloride to isophthalaldehyde. Then, a four nuclear palladacycle complex {Pd4[(N,C)(NOHCHC6H2CHNOH)(μ-Cl)2]su
Novel isoxazoline ligand with ferrocene backbone: Preparation and application in Heck reaction with water as solvent
Yu, Shuyan,Zhang, Zhiqin,Yu, Zhiyu,Shang, Yongjia
, p. 657 - 660 (2014/08/05)
Two novel isoxazoline N,N-bidentate ligands with ferrocene backbone have been synthesized and employed for the palladium-catalyzed Heck coupling reaction. Among them, 1,3-bis-(5-ferrocenylisoxazoline-3-yl)benzene was found to be thermally stable and a highly effective ligand for Heck coupling reaction in neat water without N2 protection, affording the desired coupling products in good to excellent yield with high diastereoselectivity. The developed catalytic system was also well workable for 1,2-disubstituted alkenes, which were less involved in the Heck reaction for its larger steric hindrance. Copyright
Synthesis of isoxazoles by hypervalent iodine-induced cycloaddition of nitrile oxides to alkynes
Jawalekar, Anup M.,Reubsaet, Erik,Rutjes, Floris P. J. T.,Van Delft, Floris L.
supporting information; experimental part, p. 3198 - 3200 (2011/05/05)
Treatment of oximes with hypervalent iodine leads to substituted isoxazoles via rapid formation of nitrile oxides. Reaction with terminal alkynes led to a series of 3,5-disubstituted isoxazoles with complete regioselectivity and high yield, in a procedure
