62089-34-3

Basic information

• Product Name: 3-Methoxy-5-methylbenzoic acid
• Synonyms: (3-Methoxy-5-methylphenyl)methanol
• CAS NO: 62089-34-3
• Molecular Formula: C₉H₁₀O₃
• Molecular Weight: 166.175
• Mol File: 62089-34-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: 130-131 °C
• Boiling Point: 311.5 °C at 760 mmHg
• Flash Point: 127 °C
• Appearance: /
• Density: 1.168 g/cm³
• Vapor Pressure: 0.00024mmHg at 25°C
• Refractive Index: 1.54
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.15±0.10(Predicted)
• CAS DataBase Reference: 3-Methoxy-5-methylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Methoxy-5-methylbenzoic acid(62089-34-3)
• EPA Substance Registry System: 3-Methoxy-5-methylbenzoic acid(62089-34-3)

Safety Data

• Hazardous Substances Data: 62089-34-3(Hazardous Substances Data)

Usage

General Description

3-Methoxy-5-methylbenzoic acid is a chemical compound with the molecular formula C9H10O3. It is a white to light yellow crystalline powder with a melting point of 151-155°C. 3-Methoxy-5-methylbenzoic acid is used in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential anti-inflammatory and anti-cancer properties. Additionally, 3-Methoxy-5-methylbenzoic acid has been used in the production of fragrances and flavorings due to its aromatic properties. Overall, this chemical compound has a wide range of applications in various industries.

InChI:InChI=1/C9H10O3/c1-6-3-7(9(10)11)5-8(4-6)12-2/h3-5H,1-2H3,(H,10,11)

Upstream product

• 82477-66-5 1-chloro-3-methoxy-5-methylbenzene 
• 33719-74-3 3,5-dichloroanisole 
• 15719-64-9 methylammonium carbonate 
• 585-81-9 3-hydroxy-5-methylbenzoic acid 
• 74-88-4 methyl iodide 
• 126922-33-6 Ethyl 3-Methoxy-5-methylbenzoate 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 108593-44-8 methyl 3-methoxy-5-methylbenzoate 
• 104296-19-7 2-ethyl-5-methoxy-3-methyl-benzoic acid 
• 96227-40-6 5-methoxy-3-methylbenzoic acid chloride 
• 124908-71-0 3-Methoxy-5-methyl-cyclohexa-2,5-dienecarboxylic acid 
• 119650-44-1 (3-methoxy-5-methylphenyl)methanol 
• 90674-26-3 3-methoxy-5-methyl-benzaldehyde 
• 105259-58-3 3-Methoxy-5-methylbenzoic acid diethylamide 
• 161620-96-8 3-Methoxy-5-methylbenzoic acid tert-butylamide 
• 137039-33-9 5-Hydroxy-2-<2-<(tert-butylamino)carbonyl>-6-methoxy-4-methylphenyl>-1,4-naphthoquinone 
• 161621-04-1 5-Hydroxy-2-<6-methoxy-4-methyl-2-<(diethylamino)carbonyl>phenyl>-1,4-naphthoquinone 
• 161621-05-2 3-Amino-5-hydroxy-2-<6-methoxy-4-methyl-2-<(diethylamino)carbonyl>phenyl>-1,4-naphthoquinone 
• 70351-73-4 (2-carboxy-6-methoxy-4-methylphenyl)acetic acid 
• 96227-33-7 2-(3-methoxy-5-methylphenyl)-4,4-dimethyl-Δ²-oxazoline 
• 96227-34-8 2-(3-methoxy-2,5-dimethylphenyl)-4,4-dimethyl-2-oxazoline 

Relevant articles and documents

DERIVATIVES OF 1 H-PYRAZOLO[3,4-B]PYRIDINE AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF PROLIFERATIVE DISORDERS

The present invention discloses compounds according to Formula (I): wherein R1, R2, R3, R4, L, and X are as defined herein. The present invention relates to compounds,methods for their production, pharmaceutical

Syntheses of fenanthroviridone, gilvocarcin BE-12406X2, and antibiotic WS 599B based on the palladium and copper catalyzed coupling of organostannanes with bromoquinones

A total synthesis of fenanthroviridone, gilvocarcin BE-12406X2, antibiotic WS 5995B is described based on the palladium and copper catalyzed coupling reaction of sterically hindered aryl stannanes with a 2-bromonaphthoquinone. Copyright (C) 199

A New Synthesis of Defucogilvocarcin M

A convergent synthesis of the title compound is described.The synthesis revolves around a MAD-mediated coupling of oxazoline 11 and naphthoquinone ketal 16 and requires eight steps via the longest linear sequence.