67639-61-6

Basic information

• Product Name: 2-METHOXY-3-METHYLBENZALDEHYDE
• Synonyms: 2-METHOXY-3-METHYLBENZALDEHYDE
• CAS NO: 67639-61-6
• Molecular Formula: C₉H₁₀O₂
• Molecular Weight: 150.17
• Product Categories: Aromatic Aldehydes & Derivatives (substituted)
• Mol File: 67639-61-6.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 120 °C(Press: 6 Torr)
• Appearance: /
• Density: 1.062±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-METHOXY-3-METHYLBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXY-3-METHYLBENZALDEHYDE(67639-61-6)
• EPA Substance Registry System: 2-METHOXY-3-METHYLBENZALDEHYDE(67639-61-6)

Safety Data

• Hazardous Substances Data: 67639-61-6(Hazardous Substances Data)

Usage

General Description

2-Methoxy-3-methylbenzaldehyde is a chemical compound with the molecular formula C9H10O2. It is an aromatic aldehyde with a pale yellow color and a sweet, floral odor. 2-METHOXY-3-METHYLBENZALDEHYDE is commonly used as a fragrance ingredient in perfumes and personal care products. It is also utilized in the production of flavors and fragrances for use in foods, beverages, and cosmetics. 2-Methoxy-3-methylbenzaldehyde can be synthesized from chemical precursors or extracted from natural sources such as flowers and plants. It is important to handle this compound with caution, as it can cause irritation to the skin, eyes, and respiratory system if not handled properly.

Upstream product

• 854633-33-3 2-methoxy-3-methyl-benzoic acid anilide 
• 135-02-4 ortho-anisaldehyde 
• 74-88-4 methyl iodide 
• 74090-48-5 (2-methoxy-3-methylphenyl)methanol 
• 77-78-1 dimethyl sulfate 
• 824-42-0 2-methoxy-3-methylbenzaldehyde 
• 52239-62-0 methyl 2-methoxy-3-methylbenzoate 
• 26507-91-5 2-methoxy-3-methylbenzoic acid 
• 288154-71-2 2-methoxy-3-methylbenzhydrazide 

Downstream Products

• 1951-38-8 2-methoxyisophthalic acid 
• 122950-68-9 trans-2-methoxy-3-methylstilbene 
• 74098-89-8 2-methoxy-3-methylcinnamic acid 
• 24973-35-1 1-(2-Methoxy-3-methylphenyl)-2-nitropropen 
• 882533-00-8 tris-(2-methoxy-3-methyl-benzyl)-amine 
• 111637-27-5 tri-(2-hydroxy-3-methylbenzyl)amine 
• 74090-49-6 3-(2-methoxy-3-methylphenyl)propionic acid 
• 74090-50-9 ethyl 3-(2-methoxy-3-methylphenyl)propionate 
• 74098-90-1 2-(2-methoxy-3-methylphenyl)ethyl methylsulfinylmethyl ketone 
• 74090-51-0 Ethyl-(5-methoxy-6-methyl-1,2,3,4-tetrahydro-naphthalen-2-yl)-amine 
• 769069-83-2 Benzyl-(5-methoxy-6-methyl-1,2,3,4-tetrahydro-naphthalen-2-yl)-amine 
• 606-19-9 2-hydroxyisophthalic acid 

Relevant articles and documents

Design and synthesis of a library of BODIPY-based environmental polarity sensors utilizing photoinduced electron-transfer-controlled fluorescence ON/OFF switching

We systematically examined the mechanism of the solvent polarity dependence of the fluorescence ON/OFF threshold of the BODIPY (boron dipyrromethene) fluorophore and the role of photoinduced electron transfer (PeT). In a series of BODIPY derivatives with

Nucleophilic Amination of Methoxy Arenes Promoted by a Sodium Hydride/Iodide Composite

A method for the nucleophilic amination of methoxy arenes was established by using sodium hydride (NaH) in the presence of lithium iodide (LiI). This method offers an efficient route to benzannulated nitrogen heterocycles. Mechanistic studies showed that the reaction proceeds through an unusual concerted nucleophilic aromatic substitution.

Highly Active Multidentate Catalysts for Efficient Alkyne Metathesis

The invention relates to highly active and selective catalysts for alkyne metathesis. In one aspect, the invention includes a multidentate organic ligand wherein one substrate-binding site of the metal center is blocked. In another aspect, the invention includes N-quaternized or silane-based multidentate organic ligands, capable of binding to metals. In yet another aspect, the invention includes N-quaternized or silane-based multidentate catalysts. The catalysts of the invention show high robustness, strong resistance to small alkyne polymerization and significantly enhanced catalytic activity compared to their corresponding non-quaternized or non-silane-based multidentate catalyst analogues.