5769-33-5

Basic information

• Product Name: 2,6-Dimethyl-4-bromobenzaldehyde
• Synonyms: 2,6-Dimethyl-4-bromobenzaldehyde;4-Bromo-2,6-dimethylbenzaldehyde
• CAS NO: 5769-33-5
• Molecular Formula: C₉H₉BrO
• Molecular Weight: 213.07
• Mol File: 5769-33-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 137-139 °C(Press: 12 Torr)
• Appearance: /
• Density: 1.422±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2,6-Dimethyl-4-bromobenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dimethyl-4-bromobenzaldehyde(5769-33-5)
• EPA Substance Registry System: 2,6-Dimethyl-4-bromobenzaldehyde(5769-33-5)

Safety Data

• Hazardous Substances Data: 5769-33-5(Hazardous Substances Data)

Usage

General Description

2,6-Dimethyl-4-bromobenzaldehyde is a chemical compound with the molecular formula C9H9BrO. It is a yellow-colored solid substance that is often used as an intermediate in the synthesis of pharmaceuticals and organic compounds. 2,6-Dimethyl-4-bromobenzaldehyde is commonly utilized in the production of dyes, perfumes, and other aromatic chemicals. It has also been studied for its potential use in medicinal applications, particularly in the development of anti-cancer and anti-inflammatory drugs. Additionally, 2,6-Dimethyl-4-bromobenzaldehyde is known for its strong, pungent odor and is therefore often used in the manufacturing of fragrances and flavors.

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 556-96-7 5-bromo-1,3-xylene 
• 68-12-2 N,N-dimethyl-formamide 
• 206559-43-5 5-bromo-2-iodo-1,3-dimethyl-benzene 
• 5757-66-4 4-bromo-2,6-dimethylbenzonitrile 

Downstream Products

• 159152-22-4 2,6-dimethyl-4-<2-(trimethylsilyl)ethynyl>benzaldehyde 
• 17100-59-3 (4-bromo-2,6-dimethylphenyl)methanol 

Relevant articles and documents

Spectroscopic Signatures of Resonance Inhibition Reveal Differences in Donor-Bridge and Bridge-Acceptor Couplings

The torsional dependence of the ground state magnetic exchange coupling (J) and the corresponding electronic coupling matrix element (HDA) for eight transition metal complexes possessing donor-acceptor (D-A) biradical ligands is presented. These biradical ligands are composed of an S = 1/2 metal semiquinone (SQ) donor and an S = 1/2 nitronylnitroxide (NN) acceptor, which are coupled to each other via para-phenylene, methyl-substituted para-phenylenes, or a bicyclo[2.2.2]octane ring. The observed trends in electronic absorption and resonance Raman spectral features are in accord with a reduction in electronic and magnetic coupling between D and A units within the framework of our valence bond configuration interaction model. Moreover, our spectroscopic results highlight different orbital mechanisms that modulate coupling in these complexes, which is not manifest in the ferromagnetic JSQ-B-NN values. The work provides new detailed insight into the effects of torsional rotations which contribute to inhomogeneities in experimentally determined exchange couplings, electron transfer rates, and electron transport conductance measurements.

SUBSTITUTED TRICYCLIC COMPOUNDS WITH ACTIVITY TOWARDS EP1 RECEPTORS

The present invention belongs to the field of EPl receptor ligands. More specifically it refers to compounds of general formula (I) having great affinity and selectivity for the EPl receptor. The invention also refers to the process for their preparation, to their use as medicament for the treatment and/or prophylaxis of diseases or disorders mediated by the EPl receptor as well as to pharmaceutical compositions comprising them.

A direct and mild formylation method for substituted benzenes utilizing dichloromethyl methyl ether-silver trifluoromethanesulfonate

A silver trifluoromethanesulfonate (AgOTf)-promoted direct and mild formylation of benzenes has been developed. The reaction utilizing dichloromethyl methyl ether (Cl2CHOMe) and AgOTf powerfully formylated various substituted benzenes under temperature conditions as low as -78 C without losing the protecting groups on the phenolic hydroxyl group.