Reputable Manufacturer Supply 99% Pure 67713-23-9 2,6-Dibromobenzaldehyde with Efficient Shipping

Q: What is the 2,6-Dibromobenzaldehyde?

2,6-Dibromobenzaldehyde is , while it's Molecular Formula is C7H4Br2O.

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CasNo： 67713-23-9
Molecular Formula： C₇H₄Br₂O
Purity： 99%

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What is the 2,6-Dibromobenzaldehyde ?

2,6-Dibromobenzaldehyde is a common bromine-containing aromatic aldehyde compound that has useful applications in organic synthesis, while it's Molecular Formula is C7H4Br2O.

What is the CAS number for 2,6-Dibromobenzaldehyde ?

The CAS number of 2,6-Dibromobenzaldehyde is 67713-23-9.

What is 2,6-Dibromobenzaldehyde (67713-23-9) used for?

The versatile nature of 2,6-Dibromobenzaldehyde, with its halogenated aromatic structure and aldehyde functionality, makes it a valuable compound in organic synthesis, pharmaceutical development, analytical chemistry, and materials science research.

InChI:InChI=1/C7H4Br2O/c8-6-2-1-3-7(9)5(6)4-10/h1-4H

Articles related to 2,6-Dibromobenzaldehyde:

Article

Abstract

Improved synthesis of sterically encumbered multibrominated corroles

, Chinese Chemical Letters Volume 25, Issue 10, October 2014, Pages 1349-1353

Among various types of corroles, the superstructured bis-picket-fence corroles derived from 2,6-dibromobenzaldehyde may serve as excellent non-natural porphyrinoids for use in catalytic studies, coordination chemistry and heme-protein analogues. These brominated corroles also offer an easy approach towards bis-pocket bulky corroles via functionalization by Suzuki cross-coupling reaction.

Design and synthesis of 2-(2, 6-dibromophenyl)-3-heteroaryl-1, 3-thiazolidin-4-ones as anti-HIV agents

, European Journal of Medicinal Chemistry Volume 43, Issue 12, December 2008, Pages 2800-2806

2,6-Dibromobenzaldehyde (3) was synthesized following the literature procedure [27] as shown in Scheme 1. In this procedure, 2,6-dibromoaniline (1) was diazotized by using H2SO4 and NaNO2 at −5 °C, then the cold solution of diazonium salt was neutralized by NaOAc and treated with formaldoxime solution followed by reflux in 50% H2SO4 in water to obtain the aldehyde (3). The commercially unavailable heteroaromatic amines namely, 4-methy-6-trifluoromethylpyrimidin-2-ylamine (4l),