608-96-8 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of 1,2,3,4,5-Pentaiodobenzene.
Explanation
The physical state describes the appearance and form of the compound at room temperature.
Explanation
The compound poses a significant health risk and can cause severe harm or death if ingested, inhaled, or absorbed through the skin.
Explanation
The compound can easily participate in chemical reactions, making it useful in various industrial applications.
Explanation
These are the types of chemical reactions that 1,2,3,4,5-Pentaiodbenzene can undergo, contributing to its versatility in industrial applications.
Explanation
Due to its toxic and reactive nature, it is essential to follow safety protocols when handling and storing 1,2,3,4,5-Pentaiodobenzene to prevent accidents and environmental contamination.
Physical state
Colorless solid
Toxicity
Highly toxic
Applications
a. Manufacturing of industrial products
b. Pharmaceuticals
c. Polymers
d. Production of dyes
e. Catalyst in organic synthesis
Reactivity
Highly reactive
Chemical reactions
a. Substitution
b. Addition
c. Oxidative processes
Safety precautions
Handle with caution and store properly
Check Digit Verification of cas no
The CAS Registry Mumber 608-96-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 608-96:
(5*6)+(4*0)+(3*8)+(2*9)+(1*6)=78
78 % 10 = 8
So 608-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C6HI5/c7-2-1-3(8)5(10)6(11)4(2)9/h1H
608-96-8Relevant academic research and scientific papers
Polyiodination on benzene at room temperature. A regioselective synthesis of derivatives
Barluenga,Gonzalez,Garcia-Martin,Campos
, p. 3893 - 3896 (2007/10/02)
Reaction of IPy2BF4 with benzene and CF3SO3H in CH2Cl2 gives regioselectively polyiodinated compounds at room temperature, providing a definitely easy synthetic entry to those rarely accessible benzene derivatives.
Direct Polyiodination of Benzenesulfonic Acid
Mattern, Daniell Lewis,Chen, Xinhua
, p. 5903 - 5907 (2007/10/02)
Direct aromatic polyiodination of benzenesulfonic acid (using I2 and H5IO6 in H2SO4 at room temperature) was performed to test the possible intermediacy of C6H5SO3H in the corresponding direct polyiodination of benzene to C6H2I4.The major product from C6H5SO3H was 3,4,5-triiodobenzenesulfonic acid (4).In contrast, no 4 was formed in the C6H6 reaction, showing that no significant sulfonation of C6H6 to C6H5SO3H occurred during benzene iodination.Compound 4 itself was shown to be inert under the reaction conditions.A pathway is proposed from C6H5SO3H to the other reaction products (C6I6, C6I5H, two C6I4H2 isomers, and 3,4,5-triiodophenol), which therefore avoids the intermediacy of 4.
