5025-59-2

Basic information

• Product Name: 2-IODO-6-METHOXY-BENZALDEHYDE
• Synonyms: 2-IODO-6-METHOXY-BENZALDEHYDE;Benzaldehyde, 2-iodo-6-methoxy-
• CAS NO: 5025-59-2
• Molecular Formula: C₈H₇IO₂
• Molecular Weight: 262.04
• Mol File: 5025-59-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-IODO-6-METHOXY-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-IODO-6-METHOXY-BENZALDEHYDE(5025-59-2)
• EPA Substance Registry System: 2-IODO-6-METHOXY-BENZALDEHYDE(5025-59-2)

Safety Data

• Hazardous Substances Data: 5025-59-2(Hazardous Substances Data)

Usage

General Description

2-Iodo-6-methoxy-benzaldehyde is a chemical compound with the molecular formula C8H7IO2. It is an aromatic aldehyde with a white to light yellow crystalline appearance. 2-IODO-6-METHOXY-BENZALDEHYDE is used primarily as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also utilized in the production of dyes and other organic compounds. 2-Iodo-6-methoxy-benzaldehyde is known for its strong odor and is considered to be hazardous if ingested or inhaled. As a result, it should be handled with care and in compliance with safety regulations.

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 
• 626-02-8 3-Iodophenol 
• 877265-22-0 (2-iodo-6-methoxyphenyl)methanol 
• 66195-39-9 N-benzyl-2-iodo-6-methoxybenzamide 
• 135-02-4 ortho-anisaldehyde 
• 124639-28-7 2-(2-methoxyphenyl)-1,3-dimethylimidazolidine 

Downstream Products

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

Relevant articles and documents

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.

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.

The Reimer-Tiemann reaction of m-iodophenol.

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