24063-27-2

Basic information

• Product Name: 4,6-Dibromoisophthalic acid
• Synonyms: 4,6-Dibromoisophthalic acid
• CAS NO: 24063-27-2
• Molecular Formula: C₈H₄Br₂O₄
• Molecular Weight: 323.92
• Mol File: 24063-27-2.mol
• Article Data: 15

Chemical Properties

• Melting Point: 250-254 °C
• Boiling Point: 444.9±45.0 °C(Predicted)
• Appearance: /
• Density: 2.205±0.06 g/cm3(Predicted)
• PKA: 1.95±0.10(Predicted)
• CAS DataBase Reference: 4,6-Dibromoisophthalic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-Dibromoisophthalic acid(24063-27-2)
• EPA Substance Registry System: 4,6-Dibromoisophthalic acid(24063-27-2)

Safety Data

• Hazardous Substances Data: 24063-27-2(Hazardous Substances Data)

Upstream product

• 100960-64-3 2,4-dibromo-5-methyl-benzoic acid 
• 615-87-2 1,5-dibromo-2,4-dimethylbenzene 
• 108-38-3 m-xylene 

Downstream Products

• 90766-77-1 dimethyl 4,6-dibromobenzene-1,3-dioate 
• 99361-74-7 4,6-dinitro-isophthalic acid dimethyl ester 
• 91997-32-9 4,6-dibromobenzene-1,3-dicarboxylic acid dichloride 
• 15926-89-3 4,6-dianilino-isophthalic acid 
• 861327-94-8 4,6-diphenoxy-isophthalic acid 
• 7168-99-2 4,6-dimethoxy-isophthalic acid 
• 915224-50-9 diethyl 4,6-dibromoisophthalate 
• 915224-43-0 4,6-di-thiophen-2-yl-isophthalic acid diethyl ester 
• 102467-69-6 1,5-dibromo-2,4-di-p-toluoyl-benzene 
• 113750-63-3 1,5-dibromo-2,4-bis-(2,4-dimethyl-benzoyl)-benzene 
• 114508-68-8 4,6-bis-(2,4-dimethyl-benzoyl)-m-phenylenediamine 
• 113750-29-1 1,5-dibromo-2,4-bis-(2,5-dimethyl-benzoyl)-benzene 
• 5905-36-2 N,N'-diphenyl-m-phenylenediamine 
• 7200-50-2 4,6-Dimethoxy-1,3-bis-diazoacetyl-benzol 

Relevant articles and documents

Synthesis and properties of novel N,C,N terdentate skeleton based on 1,3-di(pyridin-2-yl)benzene moiety—new tricks for old dogs

Utilization of intermolecular Friedel–Crafts and intramolecular condensation reaction, novel 1,3-di(pyridine-2-yl)benzene(N,C,N terdentate) skeleton with electro-withdrawing group in 6' position of pyridyl and a cyclization between 6' position of pyridyl and 6 position of benzyl ring were firstly designed and synthesized. The structures of these novel N,C,N terdentate were confirmed by NMR, MS and X-ray single crystalanalyses. The photophysical properties of these compounds were briefly explored.

The structure-property relationship study of electron-deficient dihydroindeno[2,1-b]fluorene derivatives for n-type organic field effect transistors

A bridged syn triphenylene derivative, namely 5,7-dihydroindeno[2,1-b]fluorene, functionalized with dicyanovinylene units (2,1-b)-IF(=C(CN)2)2 has been designed, synthesized and characterized. Its optical and electrochemical properti

Luminescent Anion Sensing by Transition-Metal Dipyridylbenzene Complexes Incorporated into Acyclic, Macrocyclic and Interlocked Hosts

A series of novel acyclic, macrocyclic and mechanically interlocked luminescent anion sensors have been prepared by incorporation of the isophthalamide motif into dipyridylbenzene to obtain cyclometallated complexes of platinum(II) and ruthenium(II). Both

Singlet Biradical Versus Triplet Biradical/Zwitterion Characteristics in Isomers of C6?C5?C6?C7?C6-Fused Pentacyclic Aromatic Hydrocarbons Revealed through Reactivity Patterns

Among various polycyclic aromatic hydrocarbons, C6?C5?C6?C7?C6 fused pentacyclic aromatic hydrocarbons have the unique potential to adopt quinonoid, zwitterion, singlet, or triplet biradical electroni

Superelectrophilic-initiated C-H functionalization at the β-position of thiophenes: A one-pot synthesis of trans-stereospecific saddle-shaped cyclic compounds

Superelectrophilic-initiated direct C-H functionalization of thiophenes at the β-position was developed. A series of trans-stereospecific [2,1-a]-IF-thiophene-fused cyclic compounds (4) with saddle-shaped structure were prepared in 17-30% yields through a