89244-39-3

Basic information

• Product Name: (2-Methoxy-6-Methylphenyl)Methanol
• Synonyms: (2-Methoxy-6-Methylphenyl)Methanol
• CAS NO: 89244-39-3
• Molecular Formula: C₉H₁₂O₂
• Molecular Weight: 152.19038
• EINECS: -0
• Mol File: 89244-39-3.mol
• Article Data: 8

Chemical Properties

• Melting Point: 51-52 °C
• Boiling Point: 259.0±25.0 °C(Predicted)
• Appearance: /
• Density: 1.060±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 14.44±0.10(Predicted)
• CAS DataBase Reference: (2-Methoxy-6-Methylphenyl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Methoxy-6-Methylphenyl)Methanol(89244-39-3)
• EPA Substance Registry System: (2-Methoxy-6-Methylphenyl)Methanol(89244-39-3)

Safety Data

• Hazardous Substances Data: 89244-39-3(Hazardous Substances Data)

Usage

General Description

(2-Methoxy-6-Methylphenyl)Methanol, also known as veratryl alcohol, is a chemical compound with a molecular formula of C9H12O2. It is a colorless, crystalline solid with a sweet, floral odor. (2-Methoxy-6-Methylphenyl)Methanol is often used as a building block in organic synthesis and as a precursor in the manufacturing of pharmaceuticals and fragrances. Additionally, it is commonly used as a reagent in chemical reactions, particularly in the field of organic chemistry. Veratryl alcohol is also known for its potential antioxidant and antimicrobial properties, making it a valuable ingredient in various industries, including cosmetics and personal care products.

Upstream product

• 2944-49-2 2,3-dimethylanisole 
• 6520-83-8 ethyl 2-methoxy-6-methylbenzoate 
• 1028202-56-3 4-methoxy-1,3-dihydroisobenzofuran 
• 79383-44-1 methyl 2-methyl-6-methoxybenzoate 
• 6555-40-4 ethyl 2-hydroxy-6-methylbenzoate 
• 6161-65-5 2-methoxy-6-methyl-benzoic acid 

Downstream Products

• 54884-55-8 2-methoxy-6-methyl-benzaldehyde 
• 18362-36-2 2-hydroxy-6-methylbenzaldehyde 
• 484016-52-6 1-(2'-hydroxy-6'-methylphenyl)ethanol 
• 173470-67-2 4-hydroxymethylbenzofurane 
• 89244-40-6 2-(Bromomethyl)-3-methylanisole 
• 1192172-68-1 ethyl 5-bromo-4-methylbenzofuran-2-carboxylate 

Relevant articles and documents

FXR receptor agonist

The present invention discloses an FXR receptor agonist, belongs to the technical field of medicine, and particularly relates to a compound represented by a formula (I), a pharmaceutically acceptablesalt, an ester or a stereoisomer thereof, wherein R, R, R, M, L, L1, W, A , B, Q, m and n are defined in the specification. The present invention further relates to a preparation method of the compound, a pharmaceutical preparation, and applications in preparation of drugs for treatment and/or prevention of nonalcoholic fatty liver disease, primary biliary cirrhosis, lipid metabolism disorder, diabetic complication, malignant tumors and other related diseases mediated by FXR receptors. The formula I is defined in the specification.

2-BENZYL-BENZIMIDAZOLE COMPLEMENT FACTOR B INHIBITORS AND USES THEREOF

The present invention provides a compound of formula (I) a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical comp

Regioselective reductive opening of substituted phthalans: synthetic applications

The reductive opening of substituted phthalans 6, 11, 12, 20, 21 and 28 with lithium and a catalytic amount of DTBB leads to the formation of corresponding functionalised organolithium intermediates 8, 15, 16, 23, 25 and 29+30 in a regioselective manner. The further reaction of these dianions with different electrophiles, mainly carbonyl compounds, gives the expected functionalised benzylic alcohols 9, 17, 18, 24, 26 and 31+32. The observed stereochemistry can be easily explained taking into account the values of the electron densities deduced by semiempirical PM3 calculations.