13815-89-9

Basic information

• Product Name: 1,4-BENZENEDICARBONYL DICHLORIDE,2-BROMO-
• Synonyms: 1,4-BENZENEDICARBONYL DICHLORIDE,2-BROMO-
• CAS NO: 13815-89-9
• Molecular Formula: C₈H₃BrCl₂O₂
• Molecular Weight: 281.92
• Mol File: 13815-89-9.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 158 °C(Press: 11 Torr)
• Appearance: /
• Density: 1.779±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,4-BENZENEDICARBONYL DICHLORIDE,2-BROMO-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-BENZENEDICARBONYL DICHLORIDE,2-BROMO-(13815-89-9)
• EPA Substance Registry System: 1,4-BENZENEDICARBONYL DICHLORIDE,2-BROMO-(13815-89-9)

Safety Data

• Hazardous Substances Data: 13815-89-9(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The compound is derived from benzene, a basic building block in organic chemistry.

Explanation

It is a compound that is used in chemical reactions to produce other compounds but is not the final product itself.

Explanation

The compound may pose risks to human health and must be handled with care in industrial settings.

Explanation

Due to its potential health hazards, proper handling and safety protocols are necessary when working with this compound in an industrial setting.

Derivative of benzene

Yes

Common uses

a. Manufacturing of polymers (nylon, polyester)
b. Production of various chemicals and materials
c. Synthesis of pharmaceuticals, agrochemicals, and specialized chemicals

Reactive intermediate

Yes

Health hazards

Potential health hazards

Industrial handling

Requires care and safety measures

Upstream product

• 586-35-6 2-bromo-1,4-benzenedicarboxylic acid 
• 7697-26-9 3-bromo-4-methylbenzoic acid 
• 553-94-6 4-bromo-m-xylene 

Downstream Products

• 18643-86-2 dimethyl 2-bromoterephthalate 
• 99779-62-1 2-[2-Bromo-4-(dicyano-trimethylsilanyloxy-methyl)-phenyl]-2-trimethylsilanyloxy-malononitrile 
• 154239-21-1 diethyl 2-Bromoterephthalate 
• 89980-92-7 (2-bromo-1,4-phenylene) dimethyl carbinol 
• 311768-09-9 2-(9,9-dihexylfluorenyl)-1,4-dichloromethylbenzene 
• 403699-41-2 2,2’-(2-bromo-1,4-phenylene)bis(methylene)bis(oxy)bis(tetrahydro-2H-pyran) 
• 403699-42-3 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-di(2-tetrahydropyranyloxymethyl)benzene 
• 403699-40-1 2-(9,9-dihexylfluorenyl)-1,4-dihydroxymethylbenzene 
• 403699-49-0 2-(7-methoxy-9,9-dihexylfluorenyl)-1,4-dichloromethylbenzene 
• 403699-50-3 2-(7-cyano-9,9-dihexylfluorenyl)-1,4-dichloromethylbenzene 
• 403699-47-8 2-(7-methoxy-9,9-dihexylfluorenyl)-1,4-dihydroxymethylbenzene 
• 403699-48-9 2-(7-cyano-9,9-dihexylfluorenyl)-1,4-dihydroxymethylbenzene 
• 403699-39-8 2-(9,9-dihexylfluorenyl)diethyl terephthalate 
• 403699-45-6 2-(7-methoxy-9,9-dihexylfluorenyl)-1,4-di(2-tetrahydropyranyloxymethyl)benzene 

Relevant articles and documents

Photoactivatable Fluorophore for Stimulated Emission Depletion (STED) Microscopy and Bioconjugation Technique for Hydrophobic Labels

The use of photoactivatable dyes in STED microscopy has so far been limited by two-photon activation through the STED beam and by the fact that photoactivatable dyes are poorly solvable in water. Herein, we report ONB-2SiR, a fluorophore that can be both

Intracellular Protein-Labeling Probes for Multicolor Single-Molecule Imaging of Immune Receptor-Adaptor Molecular Dynamics

Single-molecule imaging (SMI) has been widely utilized to investigate biomolecular dynamics and protein-protein interactions in living cells. However, multicolor SMI of intracellular proteins is challenging because of high background signals and other lim

BENZOXABOROLE FUNGICIDES

Compounds of formula (I) are as defined in the claims, and their use in compositions and methods for the control and/or prevention of microbial infection, particularly fungal infection, in plants and to processes for the preparation of these compounds.