160682-00-8 Usage
General Description
2,6-dimethyl-4-iodobenzonitrile is a chemical compound with the molecular formula C10H8IN. It is a yellow crystalline solid that is commonly used in organic synthesis and as a building block for pharmaceuticals. 2,6-dimethyl-4-iodobenzonitrile is a halogenated benzonitrile, which contains both iodine and carbon atoms. Its structure allows it to exhibit unique reactivity and behavior in various chemical reactions. It is important to handle 2,6-dimethyl-4-iodobenzonitrile with care, as it is toxic and may be harmful if ingested, inhaled, or in contact with skin. Its main applications include its use as a reagent in organic synthesis and as an intermediate in the production of pharmaceuticals and other fine chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 160682-00-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,6,8 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 160682-00:
(8*1)+(7*6)+(6*0)+(5*6)+(4*8)+(3*2)+(2*0)+(1*0)=118
118 % 10 = 8
So 160682-00-8 is a valid CAS Registry Number.
160682-00-8Relevant academic research and scientific papers
Soluble synthetic multiporphyrin arrays. 1. Modular design and synthesis
Wagner, Richard W.,Johnson, Thomas E.,Lindsey, Jonathan S.
, p. 11166 - 11180 (2007/10/03)
A set of porphyrin building blocks has been developed for the construction of light-harvesting model compounds and related molecular photonic devices. The porphyrins are facially encumbered to enhance solubility in organic solvents, are employed in a defi
Porphyrin building blocks for modular construction of bioorganic model systems
Lindsey, Jonathan S.,Prathapan, Sreedharan,Johnson, Thomas E.,Wagner, Richard W.
, p. 8941 - 8968 (2007/10/02)
We outline a modular building block strategy for the covalent assembly of porphyrin-containing model systems. Molecular design issues for the synthesis of porphyrin dimers, dye-porphyrin dyads, and multi-porphyrin arrays have been used to guide the develo
