1106813-84-6

Basic information

• Product Name: 2-lodo-5-Methylbenzaldehyde
• Synonyms: 2-lodo-5-Methylbenzaldehyde;2-iodo-5-Methylbenzaldehyde
• CAS NO: 1106813-84-6
• Molecular Formula: C8H7IO
• Molecular Weight: 246
• EINECS: -0
• Mol File: 1106813-84-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 276.1±28.0 °C(Predicted)
• Appearance: /
• Density: 1.764±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-lodo-5-Methylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-lodo-5-Methylbenzaldehyde(1106813-84-6)
• EPA Substance Registry System: 2-lodo-5-Methylbenzaldehyde(1106813-84-6)

Safety Data

• Hazardous Substances Data: 1106813-84-6(Hazardous Substances Data)

Usage

General Description

2-Iodo-5-Methylbenzaldehyde is a chemical compound with the molecular formula C8H7IO. It is a pale yellow crystalline solid with a strong, pungent odor. This chemical is commonly used as an intermediate in the synthesis of organic compounds and pharmaceuticals. It is also utilized in the research and development of new materials and chemical processes. Additionally, this compound has been studied for its potential biological and pharmacological activities, including its antimicrobial and anticancer properties. Its unique chemical structure and reactivity make it an important building block in various chemical and pharmaceutical applications.

Upstream product

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• 2941-78-8 2-Amino-5-methylbenzoic acid 
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Relevant articles and documents

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

Cu-Catalyzed Enantioselective Ring Opening of Cyclic Diaryliodoniums toward the Synthesis of Chiral Diarylmethanes

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Lewis Acid Catalyzed Formal Intramolecular [3 + 3] Cross-Cycloaddition of Cyclopropane 1,1-Diesters for Construction of Benzobicyclo[2.2.2]octane Skeletons

A novel Lewis acid catalyzed formal intramolecular [3 + 3] cross-cycloaddition (IMCC) of cyclopropane 1,1-diesters has been successfully developed. This supplies an efficient and conceptually new strategy for construction of bridged bicyclo[2.2.2]octane skeletons. This [3 + 3]IMCC could be run up to gram scale and from easily prepared starting materials. This [3 + 3]IMCC, together with our previously reported [3 + 2]IMCC strategy, can afford either the bicyclo[2.2.2]octane or bicyclo[3.2.1]octane skeletons from the similar starting materials by regulating the substituents on vinyl group.