2100-21-2 Usage
Structure
A benzene ring with three ethyl groups (-CH2CH3) attached at positions 1, 3, and 5, and an iodine atom (I) attached at position 2.
Derivative
It is a derivative of benzene.
Organic chemistry
Used as a reagent for various chemical reactions.
Synthesis
Used in the synthesis of other complex organic molecules.
Halogen bonding
Exhibits halogen bonding interactions due to the presence of the iodine atom.
Material design
Useful in the design of novel materials and pharmaceuticals.
Organic electronics
Studied for potential use in organic electronic devices.
Molecular machines
Investigated as a building block for the construction of molecular machines.
Functional groups
Ethyl groups (-CH2CH3) and an iodine atom (I).
Physical state
Likely a solid or a viscous liquid at room temperature, based on its molecular weight and structure.
Solubility
Soluble in organic solvents such as dichloromethane, acetone, and ethanol, due to its nonpolar nature.
Stability
Relatively stable under normal conditions, but may be sensitive to heat, light, or strong oxidizing agents.
Reactivity
Can undergo reactions such as halogenation, substitution, and addition reactions due to the presence of the benzene ring and iodine atom.
Hazards
Potential health hazards due to its iodine content, and may be harmful if ingested, inhaled, or absorbed through the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 2100-21-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2100-21:
(6*2)+(5*1)+(4*0)+(3*0)+(2*2)+(1*1)=22
22 % 10 = 2
So 2100-21-2 is a valid CAS Registry Number.
2100-21-2Relevant articles and documents
An efficient and regioselective iodination of electron-rich aromatic compounds using N-chlorosuccinimide and sodium iodide
Yamamoto, Takuya,Toyota, Kozo,Morita, Noboru
experimental part, p. 1364 - 1366 (2010/05/03)
An efficient and regioselective method for iodination of electron-rich aromatic compounds was found using N-chlorosuccinimide and sodium iodide in AcOH with short reaction times. This method is also applicable to non-benzenoid aromatic or heteroaromatic c
