116468-94-1 Usage
Chemical class
Xanthene derivatives It belongs to a group of chemical compounds derived from xanthene, which is a tricyclic aromatic hydrocarbon.
Molecular structure
Polycyclic aromatic compound It consists of two benzene rings fused with a xanthene ring, forming a complex and planar structure.
Functional groups
Hydroxy and phenyl groups The presence of a hydroxy (-OH) group and a phenyl group (C6H5) in the molecular structure contributes to its unique properties.
Fluorescent dye
Used in biological and chemical research Due to its fluorescent properties, it is utilized as a marker or indicator in various scientific studies.
Colorant application
Production of inks, paints, and plastics The compound's color and stability make it suitable for use as a colorant in various industries.
Organic synthesis
Potential applications in materials science Its unique structure and properties make it a candidate for further exploration in the synthesis of new materials and compounds.
Biological activities
Studied for antimicrobial and antioxidant properties Research has been conducted to understand its potential effects on biological systems, such as its ability to inhibit microbial growth and act as an antioxidant.
Stability
Relatively stable under normal conditions As a polycyclic aromatic compound, it exhibits a certain level of stability, making it suitable for various applications.
Solubility
Soluble in organic solvents Like many aromatic compounds, it is more soluble in organic solvents such as ethanol, methanol, and acetone, rather than in water.
Molecular weight
Depends on the specific molecular formula The molecular weight can be calculated based on the atomic weights of the constituent atoms and their quantities in the molecule.
Boiling point
Varies depending on the compound's structure Similar to the melting point, the boiling point is influenced by the molecular structure and intermolecular forces.
Reactivity
Can undergo various chemical reactions Due to the presence of functional groups, it can participate in reactions such as substitution, addition, and elimination.
Environmental impact
Potential ecological concerns As a synthetic compound, it may have unknown environmental effects and should be handled and disposed of according to proper guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 116468-94-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,6 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116468-94:
(8*1)+(7*1)+(6*6)+(5*4)+(4*6)+(3*8)+(2*9)+(1*4)=141
141 % 10 = 1
So 116468-94-1 is a valid CAS Registry Number.
116468-94-1Relevant articles and documents
Synthesis and self-assembly of dibenzo[jk,mn]naphtho[2,1,8-fgh]thebenidinium derivates
Wu, Dongqing,Feng, Xinliang,Takase, Masayoshi,Haberecht, Monika C.,Müllen, Klaus
experimental part, p. 11379 - 11386 (2009/04/06)
A novel synthetic method toward nitrogen containing positively charged dibenzo[jk,mn]naphtho[2,1,8-fgh]thebenidinium (DBNT, 1) salts was developed. In this method, the undehydrogenated precursor of DBNT, 14-phenyl-14-dibenzo[a,j]acridinium salt (6), was produced directly from the reaction between 14-phenyl-14-dibenzo[a,j]xanthenylium (2) and amine/aniline in reasonable yield. Various DBNT salts with different alkyl and alkylphenyl chains were synthesized in this two-step method. The self-assembly behavior of two alkylated DBNT salts, 1c and 1f, was studied in this work. Due to the different substituents and counterions, compound 1c formed nanoscale wirelike fibers, and helical aggregates were obtained from 1f, in their methanolic solutions.
