878375-85-0 Usage
Molecular structure
A long and multifaceted chemical structure containing multiple aromatic rings, amino groups, and carbon chains.
Functional groups
The presence of dione and isoindole functional groups contributes to the compound's unique properties.
Aromatic rings
The compound has multiple aromatic rings, which are characterized by their stability and delocalized electrons.
Amino groups
The presence of 4,7-diamino groups indicates that the compound has nitrogen atoms bonded to carbon atoms, which can participate in various chemical reactions and form hydrogen bonds.
Carbon chains
The compound contains long carbon chains, particularly dodecyl chains, which contribute to its hydrophobic nature.
Hydrophobicity
The presence of long carbon chains makes the compound highly hydrophobic, meaning it repels water and can interact with nonpolar molecules and surfaces.
Potential applications
Due to its intricate structure and properties, the compound has potential uses in pharmaceuticals, materials science, and other advanced applications.
Stereochemistry
The compound exhibits stereochemistry, as indicated by the (1E) and (2S) notations, which describe the spatial arrangement of atoms in the molecule.
Methylbutoxy groups
The presence of 2,5-bis[(2S)-2-methylbutoxy]phenyl groups suggests that the compound has a branched structure, which can influence its physical and chemical properties.
Ethoxy groups
The compound contains tris(dodecyloxy)phenyl groups, which are responsible for the long ethoxy chains that contribute to its hydrophobicity.
Check Digit Verification of cas no
The CAS Registry Mumber 878375-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,3,7 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 878375-85:
(8*8)+(7*7)+(6*8)+(5*3)+(4*7)+(3*5)+(2*8)+(1*5)=240
240 % 10 = 0
So 878375-85-0 is a valid CAS Registry Number.
878375-85-0Relevant academic research and scientific papers
Sinkeldam, Renatus W.,Van Houtem, Michel H. C. J.,Koeckelberghs, Guy,Vekemans, Jef A. J. M.,Meijer
, p. 383 - 385 (2006)
Herein, we report an improved methodology for the synthesis of a variety of 3,6-diaminophthalimides in high yields. This enables decoration of the periphery of foldamers with a wide range of functionalities.
Chiral alignment of OPV chromophores: Exploitation of the ureidophthalimide-based foldamer
Sinkeldam, Renatus W.,Hoeben, Freek J. M.,Pouderoijen, Maarten J.,De Cat, Inge,Zhang, Jian,Furukawa, Shuhei,De Feyter, Steven,Vekemans, Jef A. J. M.,Meijer
, p. 16113 - 16121 (2007/10/03)
The ability of foldamers to adopt a secondary structure in solution has been exploited to organize peripheral functionality. Our previously reported poly(ureidophthalimide) foldamer proved to be an excellent scaffold for the chiral organization of periphe
