38064-90-3

Basic information

• Product Name: 2,4-DIMETHOXYTOLUENE
• Synonyms: 2,4-DIMETHOXYTOLUENE;2,4-Dimethoxy-1-methylbenzene;Benzene, 1,3-dimethoxy-4-methyl;Benzene, 2,4-dimethoxy-1-methyl-
• CAS NO: 38064-90-3
• Molecular Formula: C₉H₁₂O₂
• Molecular Weight: 152.19
• Product Categories: Aromatic Hydrocarbons (substituted) & Derivatives;Anisoles, Alkyloxy Compounds & Phenylacetates;D;Stains and Dyes;Stains&Dyes, A to
• Mol File: 38064-90-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 110-120 °C30 mm Hg(lit.)
• Flash Point: 199 °F
• Appearance: /
• Density: 1.036 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.271mmHg at 25°C
• Refractive Index: n20/D 1.524(lit.)
• Storage Temp.: room temp
• CAS DataBase Reference: 2,4-DIMETHOXYTOLUENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DIMETHOXYTOLUENE(38064-90-3)
• EPA Substance Registry System: 2,4-DIMETHOXYTOLUENE(38064-90-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: NA 1993 / PGIII
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 38064-90-3(Hazardous Substances Data)

Usage

General Description

2,4-dimethoxytoluene is a chemical compound with the molecular formula C9H12O2. It is a colorless liquid with a strong odor and is commonly used as a solvent in various industrial and commercial applications. It is also used in the production of chemicals, pharmaceuticals, and other products. 2,4-dimethoxytoluene is flammable and may be harmful if inhaled or ingested, and can cause skin and eye irritation. It is important to handle and store this chemical compound with proper safety measures to prevent any potential hazards.

InChI:InChI=1/C9H12O2/c1-7-4-5-8(10-2)6-9(7)11-3/h4-6H,1-3H3

Upstream product

• 17715-69-4 1-Bromo-2,4-dimethoxybenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 496-73-1 4-methyl resorcinol 
• 77-78-1 dimethyl sulfate 
• 20469-63-0 1-iodo-2,4-dimethoxybenzene 
• 616-38-6 carbonic acid dimethyl ester 
• 82477-57-4 2-chloro-4,6-dimethoxy-3-methylaniline 
• 13362-33-9 2-methyl-1,4-benzoquinone 4-oxime 
• 7664-93-9 sulfuric acid 
• 23438-23-5 4-hydroxy-4-methyl-cyclohexa-2,5-dienone 
• 917-54-4 methyllithium 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 82477-58-5 2-chloro-4,6-dimethoxytoluene 
• 67-56-1 methanol 

Downstream Products

• 7149-91-9 2,4-dimethoxy-5-methyl-benzaldehyde 
• 77942-24-6 2',4'-dimethoxy-5'-methylpropiophenone 
• 85034-00-0 1-chloro-2,4-dimethoxy-5-methylbenzene 
• 923556-77-8 C₁₆H₂₅NO₃ 
• 91-52-1 2,4 dimethoxybenzoic acid 
• 1402588-86-6 C₅₀H₇₉NO₁₂Si₂ 
• 1402588-85-5 C₅₈H₈₇NO₁₃Si₂ 
• 1402588-84-4 C₅₁H₈₃NO₁₂Si₂ 
• 1402589-26-7 C₅₁H₈₃NO₁₂Si₂ 

Relevant articles and documents

KRAS G12D INHIBITORS

The present invention relates to compounds that inhibit KRas G12D. In particular, the present invention relates to compounds that inhibit the activity of KRas G12D, pharmaceutical compositions comprising the compounds and methods of use therefor.

A solvent-controlled highly efficient Pd-C catalyzed hydrogenolysis of benzaldehydes to methylbenzenes via a novel 'acetal pathway'

Pd-C catalyzed hydrogenolysis of benzaldehydes to methylbenzenes has been described to proceed via a 'benzenemethanol pathway'. In this article, a novel 'acetal pathway' was first revealed by a systematic study when lower alcohols were used as solvents and a solvent-controlled highly efficient procedure was established.

The Synthesis of Mycophenolic Acid from 2,4-Dihydroxybenzoic Acid

Mycophenolic acid (1) has been synthesized from 2,4-dihydroxybenzoic acid by regioselective introduction of the three required carbon substituents.A key transformation in this sequence is the introduction of the methyl substituent at position 5 by a rapid, uncatalyzed replacement of the bromide in 8 at low temperature by methyllithium.The scope and mechanism of this methylation reaction are examined.