15396-37-9

Usage

Uses

Used in Pharmaceutical Industry:
3,5-Dichloro-2-iodo-benzoic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with enhanced properties and therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, 3,5-Dichloro-2-iodo-benzoic acid is utilized as an intermediate in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Dye Industry:
3,5-Dichloro-2-iodo-benzoic acid is employed as an intermediate in the synthesis of dyes, where its unique chemical structure allows for the creation of a variety of colorants used in different applications.
Used in Research and Development:
3,5-Dichloro-2-iodo-benzoic acid is used in research and development for its unique chemical properties and reactivity, enabling scientists to explore new avenues in organic chemistry and potentially discover novel applications for 3,5-DICHLORO-2-IODO-BENZOIC ACID.

InChI:InChI=1/C7H3Cl2IO2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)/p-1

Upstream product

• 2789-92-6 3,5-dichloroantranilic acid 
• 635-21-2 5-chloroanthranilic acid 
• 51-36-5 3,5-dichlorobenzoic acid 

Downstream Products

• 94923-37-2 3,5-Dichloro-2-(2,3-dichlorophenylthio)benzoic Acid 
• 42860-31-1 3,5-dichloro-2-iodobenzoyl chloride 
• 1185755-24-1 4-[(3,5-dichloro-2-iodo-benzoyl)-(4-methoxy-benzyl)-amino]-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 79332-40-4 2,3-bis<3,5-dichloro-2-(phenylthio)phenyl>propylamine 
• 94923-41-8 2,3-Bis<3,5-dichloro-2-(2,3-dichlorophenylthio)phenyl>propionitrile 
• 79332-37-9 2,3-bis<3,5-dichloro-2-(phenylthio)phenyl>propionitrile 
• 94923-38-3 3,5-Dichloro-2-(2,3-dichlorophenylthio)benzyl Alcohol 
• 79332-47-1 <3,5-dichloro-2-(phenylthio)phenyl>acetic acid 
• 79332-35-7 3,5-dichloro-2-(4-chlorophenylthio)benzyl chloride 
• 79332-33-5 3,5-dichloro-2-(4-chlorophenylthio)benzyl alcohol 
• 79332-36-8 <3,5-dichloro-2-(phenylthio)phenyl>acetonitrile 
• 79332-34-6 3,5-dichloro-2-(phenylthio)benzyl chloride 
• 79332-32-4 3,5-dichloro-2-(phenylthio)benzyl alcohol 
• 51723-53-6 1,4-dichlorodibenzothiepin 

Relevant academic research and scientific papers

One-Pot Synthesis and Conformational Analysis of Six-Membered Cyclic Iodonium Salts

Two one-pot procedures for the construction of carbon-bridged diaryliodonium triflates and tetrafluoroborates are described. Strong Br?nsted acids enable the effective Friedel-Crafts alkylation with diversely substituted o-iodobenzyl alcohol derivatives, providing diphenylmethane scaffolds, which are subsequently oxidized and cyclized to the corresponding dibenzo[b,e]iodininium salts. Based on NMR investigations and density functional theory (DFT) calculations, we could verify the so-far-undescribed existence of two stable isomers in cyclic iodonium salts substituted with aliphatic side chains in the carbon bridge.

INHIBITORS OF 11β -HYDROXYSTEROID DEHYDROGENASE TYPE 1

This invention relates to novel compounds of the Formulae I or II and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11 β-HSD l in mammals.Formula (I).

Condensed pyrazole derivatives, process for producing the same and use thereof

Novel pharmaceutical compositions for inhibiting Th2-selective immune response and pharmaceutical compositions for inhibiting cyclooxygenase comprising condensed pyrazole derivatives represented by the general formula (I): or salts thereof.

An anion-induced regio- and chemoselective acylation and its application to the synthesis of an anticancer agent

Figure presented An efficient Grignard- and organolithium-induced regio- and chemoselective anionic acylation is reported. A number of tricyclic ketones are prepared in good to excellent yields via this method. This method is complementary to the Frieldel-Crafts acylation for electron-deficient substrates. A novel anisole-based Grignard reagent was developed to effect the cyclization of sterically hindered substrates. This novel reagent has been successfully applied to the synthesis of Sch 66336, a candidate for oncologic treatment.