379711-35-0 Usage
Appearance
White crystalline solid The compound forms a white solid with a crystalline structure.
Solubility
Soluble in water and organic solvents 2,5-dibromoisophthalic acid can dissolve in both water and various organic solvents, making it suitable for use in different chemical reactions and applications.
Use as a building block
Synthesis of coordination polymers and metal-organic frameworks The compound serves as a starting material for creating complex structures, which have various applications in materials science.
Industrial applications
Manufacture of dyes, pigments, and pharmaceuticals 2,5-dibromoisophthalic acid is used in the production of colorants and drugs, highlighting its versatility in different industries.
Potential applications in materials science
Development of functional materials for electronics, optics, and catalysis The compound has the potential to be used in creating advanced materials for various technological applications.
Luminescent and fluorescent properties
Promising candidate for imaging and sensing applications The compound's ability to emit light makes it a valuable material for use in imaging and sensing technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 379711-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,9,7,1 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 379711-35:
(8*3)+(7*7)+(6*9)+(5*7)+(4*1)+(3*1)+(2*3)+(1*5)=180
180 % 10 = 0
So 379711-35-0 is a valid CAS Registry Number.
379711-35-0Relevant articles and documents
Apical functionalization of chiral heterohelicenes
Surampudi, Sravan K.,Nagarjuna,Okamoto, Daiki,Chaudhuri, Piyali D.,Venkataraman
experimental part, p. 2074 - 2079 (2012/03/27)
We describe a synthetic protocol to selectively functionalize chiral bridged triarylamines at the apical position using regioselective copper-catalyzed amination reaction. This protocol allows the coupling of diphenylamines with a sterically hindered but
A new route for the preparation of 5-hydroxyisophthalic acid
Gelmont, Mark,Oren, Jakob
, p. 591 - 596 (2013/09/06)
A new, simple and practical, two-stage process for the preparation of 5-hydroxyisophthalic acid (5-HIPA) from isophthalic acid is described. In the first stage, isophthalic acid is brominated by bromine in oleum, in the presence of an iodine catalyst, to give crude 5-bromoisophthalic acid (5-BIPA). In the second stage the crude 5-BIPA is hydrolyzed with aqueous NaOH, in the presence of a copper catalyst, to give crude 5-HIPA, with a purity of ca. 98%. Both stages of the process were optimized. A single crystallization of the crude 5-HIPA from water gives the product in a purity of more than 99%. The overall yield of pure 5-HIPA is 65-70%.
