120281-56-3 Usage
Description
2-Iodo-5-phenylpyridine is an organoiodine compound with the chemical formula C11H7IN. It is a yellow to light brown solid that serves as a versatile building block in organic synthesis. This molecule features a pyridine ring with a phenyl group and an iodine atom positioned at the 2 and 5 positions, respectively. Its unique structure endows it with the ability to form various chemical bonds with other molecules, making it a valuable reagent in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 2-Iodo-5-phenylpyridine holds potential as a molecular tool in medicinal chemistry and drug discovery research.
Uses
Used in Organic Synthesis:
2-Iodo-5-phenylpyridine is used as a building block for the synthesis of complex organic molecules. Its presence in the molecule allows for the formation of various chemical bonds, facilitating the creation of a wide range of compounds with diverse applications.
Used in Pharmaceutical Synthesis:
2-Iodo-5-phenylpyridine is employed as a reagent in the synthesis of pharmaceuticals. Its ability to form chemical bonds with other molecules makes it a valuable component in the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-Iodo-5-phenylpyridine is used as a reagent for the synthesis of agrochemicals. Its versatility in forming chemical bonds contributes to the development of effective compounds for agricultural applications.
Used in Fine Chemicals Synthesis:
2-Iodo-5-phenylpyridine is utilized in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors. Its unique structure and bonding capabilities make it an essential component in the production of these specialized chemicals.
Used in Medicinal Chemistry and Drug Discovery Research:
2-Iodo-5-phenylpyridine is used as a molecular tool in medicinal chemistry and drug discovery research. Its potential to form various chemical bonds with other molecules allows researchers to explore its applications in the development of new therapeutic agents and the study of molecular interactions.
Used in the Conversion of Alcohols to Alkyl Iodides:
2-Iodo-5-phenylpyridine is employed as a reagent for the conversion of alcohols to alkyl iodides. This transformation is an important step in various organic synthesis processes, and the use of 2-Iodo-5-phenylpyridine as a reagent facilitates this conversion, enabling the synthesis of a wide range of alkyl iodides for further chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 120281-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,8 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120281-56:
(8*1)+(7*2)+(6*0)+(5*2)+(4*8)+(3*1)+(2*5)+(1*6)=83
83 % 10 = 3
So 120281-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H8IN/c12-11-7-6-10(8-13-11)9-4-2-1-3-5-9/h1-8H
120281-56-3Relevant articles and documents
Preparation of 2-iodo-5-phenyl-pyridine method
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Paragraph 0028; 0029, (2017/03/08)
The invention provides a method for preparing 2-iodine-5-phenylpyridine and relates to the field of an industrial production technology of 2-iodine-5-phenylpyridine. The method comprises the following steps: selecting 2-chlorine-5-phenylpyridine as an ini
Benzopyran derivatives
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, (2008/06/13)
Compounds of the formula STR1 wherein R 1 is hydrogen, halogen, trifluoromethyl, nitro, cyano, lower alkyl, lower alkoxycarbonyl, lower alkylthio, lower alkylsulphonyl, lower alkanoyl, aroyl, carbamoyl, mono(lower alkyl)carbamoyl or di(lower alkyl)carbamoyl, R 2 is hydrogen, lower alkyl or phenyl, R 3 is hydrogen or lower alkyl, R 4 and R 5 each is hydrogen or R 4 is hydroxy and R 5 is hydrogen or R 4 and R 5 together are a carbon-carbon bond and R 6 is an aryl or N-heteroaryl group carrying a hydroxy group in the 2-position or, in the case of a N-heteroaryl group, also a N-oxide group in the 2-position, and pharmaceutically acceptable acid addition salts of these compounds of formula I which are basic, possess pronounced potassium channel activating activity and can be used as medicaments, particularly in the control or prevention of hypertension, congestive heart failure, angina pectoris, peripheral and cerebral vascular disease and smooth muscle disorders.
