25458-49-5

Basic information

• Product Name: 1-(METHOXYMETHOXY)-4-METHYLBENZENE
• Synonyms: 1-(METHOXYMETHOXY)-4-METHYLBENZENE;4-(Methoxymethoxy)toluene
• CAS NO: 25458-49-5
• Molecular Formula: C₉H₁₂O₂
• Molecular Weight: 152.192
• Mol File: 25458-49-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 220℃
• Flash Point: 80℃
• Appearance: /
• Density: 0.997
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-(METHOXYMETHOXY)-4-METHYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(METHOXYMETHOXY)-4-METHYLBENZENE(25458-49-5)
• EPA Substance Registry System: 1-(METHOXYMETHOXY)-4-METHYLBENZENE(25458-49-5)

Safety Data

• Hazardous Substances Data: 25458-49-5(Hazardous Substances Data)

Usage

General Description

1-(Methoxymethoxy)-4-methylbenzene, also known as 4-methoxy-1-(methoxymethoxy)benzene, is a chemical compound with the molecular formula C9H12O2. It is a colorless to light yellow liquid with a sweet, floral odor. This chemical is primarily used as a fragrance ingredient in the production of perfumes, cosmetics, and personal care products. It is also used as a flavoring agent in food products. Additionally, 1-(Methoxymethoxy)-4-methylbenzene is sometimes utilized as an intermediate in the synthesis of other chemical compounds. However, it is important to handle this chemical with caution as it can be harmful if ingested, inhaled, or absorbed through the skin, and it may cause irritation to the eyes and skin upon contact.

Upstream product

• 1121-70-6 sodium 4-methylphenoxide 
• 107-30-2 chloromethyl methyl ether 
• 106-44-5 p-cresol 
• 109-87-5 Dimethoxymethane 

Downstream Products

• 104750-60-9 2-bromo-1-(methoxymethoxy)-4-methylbenzene 
• 116138-60-4 2-hydroxy-5-methyl-thiobenzoic acid anilide 
• 116138-59-1 2-Methoxymethoxy-5-methyl-N-phenyl-thiobenzamide 
• 5533-04-0 2-(methoxymethoxy)benzaldehyde 
• 55359-68-7 2-(methoxymethoxy)-5-methylbenzaldehyde 
• 116138-51-3 methyl 2-hydroxy-5-methylbenzenecarbodithioate 
• 142011-14-1 methyl 2-methoxymethoxy-5-methyldithiobenzoate 
• 226565-90-8 (2-Methoxymethoxy-5-methyl-phenyl)-((2R,3R)-3-methyl-oxiranyl)-methanone 
• 226565-81-7 (2-Methoxymethoxy-5-methyl-phenyl)-((2R,3S)-3-propyl-oxiranyl)-methanone 
• 308365-71-1 (2-Methoxymethoxy-5-methyl-phenyl)-[(2S,3R)-3-propyl-1-(toluene-4-sulfonyl)-aziridin-2-yl]-methanone 
• 392685-59-5 bis(2-methoxymethoxy-5-methylphenyl)phenylphosphine 
• 392685-56-2 (2-methoxymethoxy-5-methylphenyl)diphenylphosphine 
• 106-44-5 p-cresol 
• 877128-35-3 (2-methoxymethoxy-5-methyl-phenyl)-phosphonic acid diethyl ester 

Relevant articles and documents

Enantiodivergent Atroposelective Synthesis of Chiral Biaryls by Asymmetric Transfer Hydrogenation: Chiral Phosphoric Acid Catalyzed Dynamic Kinetic Resolution

Reported herein is an enantiodivergent synthesis of chiral biaryls by a chiral phosphoric acid catalyzed asymmetric transfer hydrogenation reaction. Upon treatment of biaryl lactols with aromatic amines and a Hantzsch ester in the presence of chiral phosp

Rational design of latent fluorophores from water-soluble hydroxyphenyltriazine dyes suitable for lipase sensing

Derivatives of 2-(2′-hydroxy-5′-dimethylaminobenzyl)-4,6-dimethylamino-1,3,5-triazine were synthesized by an original multistep protocol that afforded, after quaternization of the N,N-dimethylaminobenzyl moiety, water-soluble fluorescent dyes. These fluor

Rhodium/chiral diene-catalyzed asymmetric 1,4-addition of arylboronic acids to arylmethylene cyanoacetates

Asymmetric 1,4-addition of arylboronic acids to (￡)-methyl 2-cyano-3-arylpropenoates proceeded in the presence of a rhodium catalyst (3 mol %) coordinated with a chiral diene ligand, (R,R)-Ph-bod*, to give high yields of the corresponding methyl 3,3-diaryl-2-cyanopropanoates with high enantioselectivity (up to 99% ee). This catalytic asymmetric transformation was applied to the asymmetric synthesis of (R)-tolterodine. American Chemical Society.