2713-28-2

Usage

Uses

Used in Organic Synthesis:
2-Fluoro-4-Iodophenol is utilized as a key building block in organic synthesis for constructing more complex molecules. Its presence of both fluorine and iodine atoms allows for versatile chemical reactions, facilitating the creation of a wide range of organic compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-Fluoro-4-Iodophenol is employed as a precursor for the development of new drugs. Its unique structure can be modified to produce bioactive molecules with potential therapeutic applications.
Used in the Production of Fine Chemicals:
2-Fluoro-4-Iodophenol is also used in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, agriculture, and specialty chemicals.
Used as a Reagent in Chemical Reactions:
Due to its reactive nature, 2-Fluoro-4-Iodophenol serves as a reagent in various chemical reactions, enabling the synthesis of new compounds and facilitating specific transformations in organic chemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Fluoro-4-Iodophenol has potential applications due to its unique structure and properties. It can be used to design and synthesize new pharmaceutical agents with improved efficacy and selectivity.
Used in Material Science:
2-Fluoro-4-Iodophenol's distinct chemical and physical properties also make it a candidate for applications in material science, where it could be used to develop new materials with specific characteristics.

InChI:InChI=1/C6H4FIO/c7-5-3-4(8)1-2-6(5)9/h1-3,9H

Upstream product

• 3824-21-3 (3-fluoro-4-methoxyphenyl) iodide 
• 367-12-4 2-fluorophenol 
• 366-99-4 3-fluoro-4-methoxyaniline 
• 1030828-91-1 2-fluoro-4-iodophenylacetate 

Downstream Products

• 366-97-2 (2-fluoro-4-iodo-phenoxy)-acetic acid 
• 1312312-61-0 2-fluoro-4-iodophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 1257107-60-0 (2-fluoro-4-iodo-phenoxy)-acetic acid ethyl ester 
• 1257107-68-8 (R)-2-[2-fluoro-4-[3-[[1-(4-fluoro-3-methoxy-phenyl)ethyl]amino]-propyl]phenoxy]acetic acid 
• 1257107-69-9 (R)-{2-Fluoro-4-[3-(1-naphthalen-1-yl-ethylamino)-propyl]-phenoxy}-acetic acid 
• 1312312-62-1 C₂₈H₂₈FNO₁₀ 
• 1312312-63-2 C₂₈H₂₇FN₂O₁₂ 
• 1312312-64-3 2-fluoro-4-(indol-1-yl)phenyl α-D-mannopyranoside 
• 56926-74-0 (E)-3-(3-fluoro-4-hydroxyphenyl)acrylic acid 
• 1505448-04-3 2-(8-(2-fluoro-4-iodophenoxy)oct-6-yn-1-yl)-2-methyl-1,3-dioxolane 
• 1610035-72-7 2-((2S,3S,4R)-1-(4-(((3,4-trans)-1-(5-chloro-2-methoxypyridin-4-yl)-3-methylpiperidin4-yl)oxy)-3-fluorophenyl)-4-methoxy-3-methylpyrrolidin-2-yl)acetic acid 
• 1610035-74-9 ((2R,3S,4R)-1-(4-(((3,4-trans)-1-(5-chloro-2-methoxypyridin-4-yl)-3-methylpiperidin-4-yl)oxy)-3-fluorophenyl)-4-methoxy-3-methylpyrrolidin-2-yl)methanol 
• 1610035-75-0 ((2R,3S,4R)-1-(4-(((3,4-trans)-1-(5-chloro-2-methoxypyridin-4-yl)-3-methylpiperidin-4-yl)oxy)-3-fluorophenyl)-4-methoxy-3-methylpyrrolidin-2-yl)methyl methanesulfonate 
• 1610035-76-1 2-((2S,3S,4R)-1-(4-(((3,4-trans)-1-(5-chloro-2-methoxypyridin-4-yl)-3-methylpiperidin-4-yl)oxy)-3-fluorophenyl)-4-methoxy-3-methylpyrrolidin-2-yl)acetonitrile 

Relevant academic research and scientific papers

TETRASUBSTITUTED ALKENE COMPOUNDS AND THEIR USE

Disclosed herein are compounds, or pharmaceutically acceptable salts thereof, and methods of using the compounds for treating breast cancer by administration to a subject in need thereof a therapeutically effective amount of the compounds or pharmaceutically acceptable salts thereof. The breast cancer may be an ER-positive breast cancer and/or the subject in need of treatment may express a mutant ER-α protein.

ORGANIC COMPOUNDS

Novel benzofuran derivatives are disclosed. The derivatives have S1P1 receptor activity and/or disease modifying activity and find use in the treatment of conditions or diseases associated with the immune, vascular and nervous systems in animals and/or humans

CALCIUM-SENSING RECEPTOR-ACTIVE COMPOUNDS

A compound of general formula I their use as calcium receptor-active compounds for the prophylaxis, treatment or amelioration of physiological disorders or diseases associated with disturbances of CaSR activity, such as hyperparathyroidism, pharmaceutical

Mild and efficient oxy-iodination of alkynes and phenols with potassium iodide and tert-butyl hydroperoxide

An efficient synthesis of 1-iodoalkynes and iodophenols was easily achieved by employing simple KI and TBHP. The reaction does not involve the use of a metal and base combination. A variety of substituted alkynes and phenols were prepared with good to excellent yield.

NOVEL PHENYL-ISOXAZOL-3-OL DERIVATIVE

The present invention relates to a compound represented by formula (I), which has a GPR120 agonist action and thus is useful for treatment of diabetes mellitus or hyperlipidemia, or a pharmaceutically acceptable salt thereof. In the formula, (AA) represents a phenyl or the like, which may be substituted with a lower alkoxy group or the like; (BB) represents a divalent group or the like, derived by removal of two hydrogen atoms from a benzene which may be substituted with a halogen atom or the like; X represents a spacer having a main chain composed of 1-8 carbon atoms wherein 1-3 carbon atoms in the main chain may be substituted with an oxygen atom or the like; and Y represents a hydrogen atom or the like.

Liquid crystal compounds and optically active compounds

A compound usefull for liquid crystal component which is represented by the following formulas (1), (2), (3), or (4) ;, R1 -X1 -A1 -( A2 )n-Y1 -A3 -X2 -R2 (1), R1 -X1 -( A3 -Y1 )N-A1 -A2 -X2 -R2 (2), R3 -X1 -A4 -Y1 -A3 -X2 -R4 (3), R3 -X1 -A5 -Y1 -A1 -A2 -X2 -R4 (4), wherein R1 ,R2 ,R3 and R4 are C1 18 alkyl groups; X1 and X2 is -, O, S, -C≡C- or divarent groups such as COO, OCO, CH2 O or OCH2