103808-42-0

Basic information

• Product Name: Benzaldehyde, 2,5-dimethoxy-3,4,6-trimethyl-
• CAS NO: 103808-42-0
• Molecular Formula: C₁₂H₁₆O₃
• Molecular Weight: 208.257
• Mol File: 103808-42-0.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 338.781 °C at 760 mmHg
• Flash Point: 149.846 °C
• Density: 1.052 g/cm³
• CAS DataBase Reference: Benzaldehyde, 2,5-dimethoxy-3,4,6-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2,5-dimethoxy-3,4,6-trimethyl-(103808-42-0)
• EPA Substance Registry System: Benzaldehyde, 2,5-dimethoxy-3,4,6-trimethyl-(103808-42-0)

Safety Data

• Hazardous Substances Data: 103808-42-0(Hazardous Substances Data)

Upstream product

• 4537-09-1 1,4-dimethoxy-2,3,5-trimethyl-benzene 
• 69821-05-2 1-bromo-2,5-dimethoxy-3,4,6-trimethylbenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 855272-69-4 1-acetoxymethyl-2,5-dimethoxy-3,4,6-trimethyl-benzene 
• 700-13-0 Trimethylhydroquinone 
• 861356-37-8 (2,5-dimethoxy-3,4,6-trimethyl-benzylidene)-malonic acid 
• 117574-74-0 (2,5-dimethoxy-3,4,6-trimethylphenyl)methanol 
• 64-19-7 acetic acid 
• 100-97-0 hexamethylenetetramine 
• 4885-02-3 Dichloromethyl methyl ether 

Downstream Products

• 117574-74-0 (2,5-dimethoxy-3,4,6-trimethylphenyl)methanol 
• 117574-75-1 1-(bromomethyl)-2,5-dimethoxy-3,4,6-trimethylbenzene 
• 87541-59-1 2-(2,5-dimethoxy-3,4,6-trimethylphenyl)ethanamine 
• 80810-61-3 4-(2,5-dimethoxy-3,4,6-trimethylphenyl)butan-1-ol 
• 174868-66-7 (2,5-Dimethoxy-3,4,6-trimethyl-phenyl)-(3-[1,3]dioxolan-2-yl-phenyl)-methanol 
• 147225-13-6 1-(4-methoxyoxazolin-5-yl)-2,5-dimethoxy-3,4,6-trimethylbenzene 

Relevant articles and documents

PREPARATION AND USES OF REACTIVE OXYGEN SPECIES SCAVENGER DERIVATIVES

Compounds of Formula (I) a or (I) b: including certain quinone derivatives, and the corresponding pharmaceutical compositions, which may serve to modulate ferroptosis in a subject. Also disclosed herein are the preparations of these compounds and pharmaceutical compositions and their potential uses in the manufacture of a medicament in reducing reactive oxygen species (ROS) in a cell and for preventing, treating, ameliorating certain related disorder or a disease.

Catalytic Asymmetric Cycloadditions of Silyl Nitronates Bearing α-Aryl Group

1,3-Dipolar cycloadditions of 2-alkylacroleins or atropaldehyde with triisopropylsilyl nitronates bearing an α-aryl group produced 3-aryl-2-isoxazolines having a chiral quaternary center in up to 94% ee and up to 88% yield with the aid of Corey’s oxazaborolidine catalyst. Specifically, the TIPS nitronate with an α-(p-methoxyphenyl) group gave mainly the 2-isoxazolines having an all-carbon quaternary center.

Enzymatic substrates derived from phenoxazinone and their use as developer in detection of microorganisms with peptidase activity

Novel enzymatic substrates of the general formula below: reaction media containing the same and their use for detecting and/or identifying and/or quantifying microorganisms expressing at least one peptidase activity.