185342-88-5

Basic information

• Product Name: 1,3-DIBROMO-2,4-DIMETHOXY-BENZENE
• Synonyms: 1,3-DIBROMO-2,4-DIMETHOXY-BENZENE
• CAS NO: 185342-88-5
• Molecular Formula: C₈H₈Br₂O₂
• Molecular Weight: 295.95592
• Mol File: 185342-88-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 90-91 °C
• Boiling Point: 155 °C(Press: 16 Torr)
• Appearance: /
• Density: 1.742±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,3-DIBROMO-2,4-DIMETHOXY-BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DIBROMO-2,4-DIMETHOXY-BENZENE(185342-88-5)
• EPA Substance Registry System: 1,3-DIBROMO-2,4-DIMETHOXY-BENZENE(185342-88-5)

Safety Data

• Hazardous Substances Data: 185342-88-5(Hazardous Substances Data)

Usage

General Description

1,3-Dibromo-2,4-dimethoxy-benzene is a synthetic, organic chemical compound characterized by the presence of bromine and methoxy functional groups attached to a benzene ring. This aromatic compound uniquely carries two bromine atoms at the 1st and 3rd positions and two methoxy groups at the 2nd and 4th positions of the benzene ring. It is primarily used in the laboratory for research and chemical synthesis, often as a starting material or an intermediate in the production of other complex organic molecules. Its physical and chemical properties, such as solubility, melting point, boiling point, and reactivity, largely depend on the bromine and methoxy substituents. Its handling and use require appropriate safety measures due to the potential hazards associated with bromine compounds.

Upstream product

• 151-10-0 1,3-Dimethoxybenzene 
• 16932-45-9 1-bromo-2,6-dimethoxybenzene 
• 18011-67-1 2,4-dibromo-1,3-benzenediol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1256544-69-0 6-(3-bromophenyl)benzofurano[2,3-c]dibenzofuran 
• 875902-97-9 1,3-dimethoxy-2,4-diformylbenzene 

Relevant articles and documents

Discovery of 2,4-dimethoxypyridines as novel autophagy inhibitors

Autophagy is a catabolic process, which mediates degradation of cellular components and has important roles in health and disease. Therefore, small molecule modulators of autophagy are in great demand. Herein, we describe a phenotypic high-content screen for autophagy inhibitors, which led to the discovery of a dimethoxypyridine-based class of autophagy inhibitors, which derive from previously reported, natural product-inspired MAP4K4 inhibitors. Comprehensive structure-activity relationship studies led to a potent compound, and biological validation experiments indicated that the mode of action was upstream or independent of mTOR.

COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

When a decrease in low-grey level region (e.g., 0 to 80 grey) efficiencies of organic light emitting devices is not constant, deviation among display panels may cause color change and stain in the low luminance region. Aspects of the present disclosure ar

ANTHRACENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT USING THE SAME

An anthracene derivative represented by the following formula (1): In the formula (1), Z is a structure represented by the following formula (2). In the formula (2), at least one pair of adjacent two substituents of R11 to R18 form a ring represented by the following formula (3) or (4):