5025-59-2

Usage

Uses

Used in Pharmaceutical Industry:
2-IODO-6-METHOXY-BENZALDEHYDE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a crucial component in the development of new drugs, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
In the agrochemical sector, 2-IODO-6-METHOXY-BENZALDEHYDE serves as an intermediate for the production of agrochemicals. Its role in this industry is vital for the development of effective and safe products for agricultural applications.
Used in Dye Production:
2-IODO-6-METHOXY-BENZALDEHYDE is utilized in the production of dyes, where its chemical properties contribute to the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing.
Used in Organic Compounds Synthesis:
2-IODO-6-METHOXY-BENZALDEHYDE is also employed in the synthesis of other organic compounds, showcasing its versatility and importance in the field of organic chemistry. Its presence in various chemical reactions highlights its value in creating new and innovative products.

InChI:InChI=1S/C8H7IO2/c1-11-8-4-2-3-7(9)6(8)5-10/h2-5H,1H3

Upstream product

• 38169-97-0 2-hydroxy-6-iodobenzaldehyde 
• 77-78-1 dimethyl sulfate 
• 19689-88-4 2-methoxy-6-nitrobenzaldehyde 
• 124639-28-7 2-(2-methoxyphenyl)-1,3-dimethylimidazolidine 
• 135-02-4 ortho-anisaldehyde 
• 66195-39-9 N-benzyl-2-iodo-6-methoxybenzamide 
• 626-02-8 3-Iodophenol 
• 877265-22-0 (2-iodo-6-methoxyphenyl)methanol 

Downstream Products

• 66195-39-9 N-benzyl-2-iodo-6-methoxybenzamide 
• 877264-41-0 C₉H₁₂INO 
• 38169-97-0 2-hydroxy-6-iodobenzaldehyde 

Relevant academic research and scientific papers

INHIBITORS OF PURINE NUCLEOSIDE PHOSPHORYLASE - SYNTHESIS AND USE THEREOF FOR TREATMENT OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA AND LYMPHOMA

The present invention relates to new compounds of general formula I, their synthesis, their pharmaceutically acceptable salts, and their use in treatment of T-cell acute lymphoblastic leukemia and lymphoma.

Monodentate Transient Directing Group-Assisted Palladium-Catalyzed Direct ortho-C-H Iodination of Benzaldehydes for Total Synthesis of Hernandial

The first palladium-catalyzed direct o-C-H iodination of benzaldehydes was successfully developed with the assistance of commercially available 2,5-bis(trifluoromethyl)aniline as the optimal monodentate transient directing group (MonoTDG). Moderate to exc

Palladium-Catalyzed, Norbornene-Mediated, ortho-Amination ipso-Amidation: Sequential C-N Bond Formation

A palladium-catalyzed, norbornene-mediated ortho- and ipso-C-N bond-forming Catellani reaction is reported. This reaction proceeds through a sequential intermolecular amination followed by intramolecular cyclization of a tethered amide. The products, ortho-aminated dihydroquinolinones, were generated in moderate to good yields and are present in bioactive molecules. This work highlights the challenge of competing intra- vs intermolecular palladium-catalyzed processes.

Aryl- and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin

The compounds of the present invention are represented by the chemical structure found in Formula (I): wherein: the carbon atom designated * is in the R or S configuration; and X is a fused bicyclic carbocycle or heterocycle selected from the group consisting of benzofuranyl, benzo[b]thiophenyl, benzoisothiazolyl, benzoisoxazolyl, indazolyl, indolyl, isoindolyl, indolizinyl, benzoimidazolyl, benzooxazolyl, benzothiazolyl, benzotriazolyl, imidazo[1,2-a]pyridinyl, pyrazolo[1,5-a]pyridinyl, [1,2,4]triazolo[4,3-a]pyridinyl, thieno[2,3-b]pyridinyl, thieno[3,2-b]pyridinyl, 1H-pyrrolo[2,3-b]pyridinyl, indenyl, indanyl, dihydrobenzocycloheptenyl, tetrahydrobenzocycloheptenyl, dihydrobenzothiophenyl, dihydrobenzofuranyl, indolinyl, naphthyl, tetrahydronaphthyl, quinolinyl, isoquinolinyl, 4H-quinolizinyl, 9aH-quinolizinyl, quinazolinyl, cinnolinyl, phthalazinyl, quinoxalinyl, benzo[1,2,3]triazinyl, benzo[1,2,4]triazinyl, 2H-chromenyl, 4H-chromenyl, and a fused bicyclic carbocycle or fused bicyclic heterocycle optionally substituted with substituents (1 to 4 in number) as defined in R14; with R1, R2, R3, R4, R5, R6, R7, R8, and R14 defined herein.