409318-68-9 Usage
Explanation
The compound's name is derived from its structure, which includes a benzene ring with two amino groups (-NH2) at the 1 and 4 positions, and two bromine atoms (Br) at the 2 and 5 positions.
Explanation
The formula represents the compound's composition, which consists of 12 carbon (C) atoms, 10 hydrogen (H) atoms, 2 bromine (Br) atoms, and 2 nitrogen (N) atoms.
Explanation
The molecular weight is the sum of the atomic weights of all the atoms in the molecule, which is approximately 342.13 grams per mole.
Explanation
The compound is typically a solid at room temperature, with a color ranging from colorless to pale yellow.
Explanation
The compound is more soluble in organic solvents due to its nonpolar nature, which allows it to dissolve in other nonpolar substances.
Explanation
As a diamine compound, it can participate in various chemical reactions, such as condensation, substitution, and addition reactions, to form new organic compounds.
Explanation
The compound's reactivity and structural features make it a valuable starting material for the synthesis of various dyes, pigments, and other chemicals.
Explanation
Due to its chemical properties, 1,4-Benzenediamine, 2,5-dibromo-N,N'-diphenylcan pose health risks if not handled with care. It is essential to follow safety guidelines and use appropriate protective measures when working with 1,4-Benzenediamine, 2,5-dibromo-N,N'-diphenyl-.
Explanation
Proper storage conditions help maintain the compound's stability and prevent accidental reactions or degradation.
Explanation
Wearing PPE minimizes the risk of exposure to the compound and potential health hazards.
Molecular Weight
342.13 g/mol
Appearance
Colorless to pale yellow solid
Solubility
Soluble in organic solvents like ethanol, acetone, and dichloromethane
Reactivity
Reacts with other chemicals to form new compounds
Applications
Used as a raw material in the production of dyes, pigments, and other chemicals
Toxicity
Can be toxic and harmful if not used properly
Storage
Store in a cool, dry, and well-ventilated area, away from heat and sources of ignition
Safety Precautions
Use personal protective equipment (PPE) such as gloves, goggles, and a lab coat when handling the compound
Check Digit Verification of cas no
The CAS Registry Mumber 409318-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,9,3,1 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 409318-68:
(8*4)+(7*0)+(6*9)+(5*3)+(4*1)+(3*8)+(2*6)+(1*8)=149
149 % 10 = 9
So 409318-68-9 is a valid CAS Registry Number.
409318-68-9Relevant academic research and scientific papers
π-Conjugated polymers exhibiting a novel doping based on redox of side chains
Nishiumi, Toyohiko,Higuchi, Masayoshi,Yamamoto, Kimihisa
, p. 6325 - 6332 (2007/10/03)
Novel polyphenylene and polythiophene derivatives that have N,N′-diphenyl-1,4-phenylene-diamine (PDA) units were synthesized using the palladium-catalyzed Suzuki coupling or cross coupling. Each obtained polymer has good redox activity, and the polyphenylene derivatives have two redox couples in acetonitrile that contain 1 M trifluoroacetric acid, whereas the polythiophene derivatives show only one redox couple under the same conditions. The electronic conductivity of the polythiophene derivatives was dramatically enhanced (0.1 S/cm) by the one-electron oxidation of the PDA unit (0.4 V, vs Ag/Ag+), because of the injection of a radical cation into the main chain from the PDA unit. Spectroelectrochemistry showed that the radical cation of the thiophene-substituted PDA was more delocalized than the phenylene-substituted unit. Electrochemical analysis of the model compounds revealed that the injection of radical monocation radical carriers into the main chain is based on electron communication between the intramolecular PDAs.
