100189-84-2

Basic information

• Product Name: 2,5-DIBROMO-M-XYLENE
• Synonyms: 2,5-DIBROMO-M-XYLENE;1,4-DIBROMO-2,6-DIMETHYLBENZENE;2,5-Dibromo-1,3-dimethylbenzene;Benzene, 2,5-dibroMo-1,3-diMethyl-
• CAS NO: 100189-84-2
• Molecular Formula: C₈H₈Br₂
• Molecular Weight: 263.96
• Product Categories: Bromine Compounds
• Mol File: 100189-84-2.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 261.7±35.0 °C(Predicted)
• Appearance: /
• Density: 1.710±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2,5-DIBROMO-M-XYLENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-DIBROMO-M-XYLENE(100189-84-2)
• EPA Substance Registry System: 2,5-DIBROMO-M-XYLENE(100189-84-2)

Safety Data

• Hazardous Substances Data: 100189-84-2(Hazardous Substances Data)

Usage

General Description

2,5-Dibromo-m-xylene is a chemical compound, more specifically an aromatic hydrocarbon. Its chemical formula is C8H8Br2. It belongs to the class of organic compounds known as bromobenzenes, which are compounds containing one or more bromine atoms attached to a benzene moecule. This chemical can be utilized in various applications within the scientific and manufacturing industries. Its safety, environmental impact, and regulatory status should be thoroughly checked according to regional regulations before use. As with many chemicals, appropriate measures should be taken to ensure safe handling and storage.

Upstream product

• 24596-19-8 4-bromo-2,6-dimethylphenylamine 
• 59557-90-3 4-bromo-3,5-dimethylaniline 
• 108-69-0 3,5-dimethylaminoaniline 
• 87-62-7 2,6-dimethylaniline 
• 576-22-7 2-Bromo-m-xylene 

Downstream Products

• 7697-32-7 4-bromo-3,5-dimethylbenzoic acid 
• 33641-91-7 1,3-Bis-(chloromethyl)-2,5-dibromo-4,6-dimethylbenzol 
• 100189-85-3 2-bromo-1,3-dimethyl<5-2H>benzene 
• 400822-47-1 4-bromo-3,5-dimethylbenzaldehyde 
• 689260-65-9 2,5-dibromo-1,3-bis(bromomethyl)benzene 
• 740815-82-1 2,5-dibromo-1,3-bis(cyanomethyl)benzene 
• 75344-77-3 4-bromo-3,5-dimethyl benzonitrile 
• 400822-49-3 4-bromo-3,5-dimethylbenzaldehyde oxime 
• 100189-86-4 1,3-dimethyl<2,5-2H2>benzene 
• 26965-70-8 4-Chlormethyl-2,6-dimethyl-brombenzol 
• 27006-02-6 (4-bromo-3,5-dimethylphenyl)methanol 
• 1265481-48-8 sodium 4-bromo-3,5-dimethylbenzoate 
• 910636-36-1 2-(4-bromo-3,5-dimethyl-phenyl)-[1,3]dioxane 
• 910636-37-2 2-(4-allyl-3,5-dimethyl-phenyl)-[1,3]dioxane 

Relevant articles and documents

Rational Design of a Near-infrared Fluorescence Probe for Ca2+ Based on Phosphorus-substituted Rhodamines Utilizing Photoinduced Electron Transfer

Fluorescence imaging in the near-infrared (NIR) region (650–900 nm) is useful for bioimaging because background autofluorescence is low and tissue penetration is high in this range. In addition, NIR fluorescence is useful as a complementary color window t

Development of a Series of Practical Fluorescent Chemical Tools to Measure pH Values in Living Samples

In biological systems, the pH in intracellular organelles or tissues is strictly regulated, and differences of pH are deeply related to key biological events such as protein degradation, intracellular trafficking, renal failure, and cancer. Ratiometric fluorescence imaging is useful for determination of precise pH values, but existing fluorescence probes have substantial limitations, such as inappropriate pKa for imaging in the physiological pH range, inadequate photobleaching resistance, and insufficiently long excitation and emission wavelengths. Here we report a versatile scaffold for ratiometric fluorescence pH probes, based on asymmetric rhodamine. To demonstrate its usefulness for biological applications, we employed it to develop two probes. (1) SiRpH5 has suitable pKa and water solubility for imaging in acidic intracellular compartments; by using transferrin tagged with SiRpH5, we achieved time-lapse imaging of pH in endocytic compartments during protein trafficking for the first time. (2) Me-pEPPR is a near-infrared (NIR) probe; by using dextrin tagged with Me-pEPPR, we were able to image extracellular pH of renal tubules and tumors in situ. These chemical tools should be useful for studying the influence of intra- and extracellular pH on biological processes, as well as for in vivo imaging.

NEAR-INFRARED FLUORESCENT RATIO TYPE PROBE

PROBLEM TO BE SOLVED: To provide a novel near-infrared fluorescent pH probe. SOLUTION: The invention provides a compound represented by general formula (I), or a salt thereof. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT