3946-40-5 Usage
Description
(6E)-6-[(2-hydroxybenzyl)amino]methylidenecyclohexa-2,4-dien-1-one is a complex cyclic ketone with a substituted cyclohexadiene ring. It features a benzylamine group attached to the cyclohexadiene ring, with a hydroxybenzyl group linked to the amine. (6E)-6-[(2-hydroxybenzyl)amino]methylidenecyclohexa-2,4-dien-1-one is in the E configuration, which refers to the positioning of the double bond in the cyclohexadiene ring. This intricate chemical structure indicates potential applications in various fields, including organic synthesis and pharmaceutical research, as well as possible biological activities that could be of interest for further studies in medicinal chemistry and drug development.
Uses
Used in Organic Synthesis:
(6E)-6-[(2-hydroxybenzyl)amino]methylidenecyclohexa-2,4-dien-1-one is used as a key intermediate for the synthesis of various organic compounds due to its complex and functionalized nature. Its unique structure allows for further chemical modifications and the creation of novel molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (6E)-6-[(2-hydroxybenzyl)amino]methylidenecyclohexa-2,4-dien-1-one is used as a starting material for the development of new drugs. Its complex structure and functional groups make it a promising candidate for the design and synthesis of innovative therapeutic agents.
Used in Medicinal Chemistry:
(6E)-6-[(2-hydroxybenzyl)amino]methylidenecyclohexa-2,4-dien-1-one is used as a compound of interest for further studies in medicinal chemistry. Its potential biological activities and the possibility of optimizing its structure for specific therapeutic applications make it a valuable subject for research and development.
Used in Drug Development:
In the field of drug development, (6E)-6-[(2-hydroxybenzyl)amino]methylidenecyclohexa-2,4-dien-1-one is used as a lead compound for the discovery of new pharmaceuticals. Its unique chemical structure and potential biological activities provide a foundation for the development of novel therapeutic agents with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 3946-40-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3946-40:
(6*3)+(5*9)+(4*4)+(3*6)+(2*4)+(1*0)=105
105 % 10 = 5
So 3946-40-5 is a valid CAS Registry Number.
3946-40-5Relevant articles and documents
Synthesis of heptanuclear Ni4Dy3 coordination aggregate using tridentate ligand: X-ray structure, magnetism and theoretical studies
Bhanja, Avik,Herchel, Radovan,Kotrle, Kamil,Murrie, Mark,Ortu, Fabrizio,Ray, Debashis,Smythe, Lucy
, (2021)
The Schiff base ligand, 2-(((2-hydroxybenzyl)imino)methyl)phenol (H2L) having ONO donor centres are utilized to synthesize {Ni4Dy3} coordination aggregate following the support of six benzoate bridging groups. Sequential a
Trans-Symmetric Dynamic Covalent Systems: Connected Transamination and Transimination Reactions
Schaufelberger, Fredrik,Hu, Lei,Ramstr?m, Olof
supporting information, p. 9776 - 9783 (2015/06/30)
The development of chemical transaminations as a new type of dynamic covalent reaction is described. The key 1,3-proton shift is under complete catalytic control and can be conducted orthogonally to, or simultaneous with, transimination in the presence of an amine to rapidly yield two-dimensional dynamic systems with a high degree of complexity evolution. The transamination-transimination systems are proven to be fully reversible, stable over several days, compatible with a range of functional groups, and highly tunable. Kinetic studies show transamination to be the rate-limiting reaction in the network. Furthermore, it was discovered that readily available quinuclidine is a highly potent catalyst for aldimine transaminations. This study demonstrates how connected dynamic reactions give rise to significantly larger systems than the unconnected counterparts, and shows how reversible isomerizations can be utilized as an effective diversity-generating element. Constant exchange: The development of chemical transaminations as a new type of dynamic covalent reactions is described (see figure). This study demonstrates how connected dynamic reactions give rise to significantly larger systems than the unconnected counterparts, and shows how reversible isomerizations can be utilized as an effective diversity-generating element.
Lanthanide(III) Complexes of ONO Donor Schiff Bases Derived from Salicylaldehyde and o-Hydroxybenzylamine or o-Aminobenzylalcohol
Syamal, A.,Maurya, M. R.
, p. 357 - 359 (2007/10/02)
Several new complexes of isomeric schiff bases derived from salicylaldehyde and o-hydroxybenzylamine/o-aminobenzylalcohol with Pr(III), Nd(III), Sm(III), Gd(III), Tb(III) and Dy(III) have been synthesized and characterized by elemental analysis, molar con
