606-19-9 Usage
Description
2-Hydroxyisophthalic acid is a benzenedicarboxylic acid derivative, specifically an isophthalic acid with a hydroxy group substituted at the 2-position. This chemical structure endows it with unique properties that make it suitable for various applications across different industries.
Uses
Used in Chemical Synthesis:
2-Hydroxyisophthalic acid is used as a key intermediate in the synthesis of various specialty chemicals and polymers. Its presence of both carboxylic acid and hydroxyl functional groups allows for versatile chemical reactions, making it a valuable building block for the production of high-performance materials.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Hydroxyisophthalic acid is utilized as a starting material for the development of novel drug candidates. Its ability to form hydrogen bonds and participate in various chemical reactions enables the creation of new compounds with potential therapeutic applications.
Used in Coatings and Adhesives:
2-Hydroxyisophthalic acid is employed as a cross-linking agent in the formulation of coatings and adhesives. Its reactive functional groups facilitate the formation of strong bonds between polymer chains, resulting in improved mechanical properties and durability of the final products.
Used in Textile Industry:
In the textile industry, 2-Hydroxyisophthalic acid is used as a component in the production of dyestuffs and finishing agents. Its chemical reactivity allows for the attachment of various functional groups, which can enhance the colorfastness, water resistance, and other properties of textiles.
Used in Agriculture:
2-Hydroxyisophthalic acid is utilized in the development of agrochemicals, such as herbicides and pesticides. Its chemical properties enable the design of compounds that can effectively control the growth of unwanted plants and pests, thereby improving crop yields and quality.
Check Digit Verification of cas no
The CAS Registry Mumber 606-19-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 606-19:
(5*6)+(4*0)+(3*6)+(2*1)+(1*9)=59
59 % 10 = 9
So 606-19-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O5/c9-6-4(7(10)11)2-1-3-5(6)8(12)13/h1-3,9H,(H,10,11)(H,12,13)
606-19-9Relevant articles and documents
Designer ligands for beryllium
Keizer, Timothy S.,Sauer, Nancy N.,McCleskey, T. Mark
, p. 9484 - 9485 (2004)
We report the rational design of ligands that selectively bind beryllium. We selected two ligands to design Be based on binding polynulear species with a Be-O-Be motif: 2-hydroxyisophthalic acid (HIPA) and 2,3-dihydroxybenzoic acid (DHBA). All previous wo
High-relaxivity Gd(III)-hemicryptophane complex
Godart, Estelle,Long, Augustin,Rosas, Roselyne,Lemercier, Gilles,Jean, Marion,Leclerc, Sébastien,Bouguet-Bonnet, Sabine,Godfrin, Célia,Chapellet, Laure-Lise,Dutasta, Jean-Pierre,Martinez, Alexandre
supporting information, p. 1999 - 2003 (2019/04/11)
The polytopic hemicryptophane cage HC1 combining a cyclotriveratrylene (CTV) unit and a tris(2-aminoethyl)amine (tren) moiety connected by three 2-hydroxyisophthalamide linkers was synthesized in 12 steps. The resulting highly functionalized covalent host
Tenacic Acids: A New Class of Tenacious Binders to Metal Oxide Surfaces
Komati, Rajesh,Mitchell, Carl A.,LeBeaud, Anastasia,Do, Huy,Goloverda, Galina Z.,Kolesnichenko, Vladimir L.
supporting information, p. 14824 - 14829 (2018/09/12)
The backbone of 2-hydroxyisophthalic acid was identified as a potential metal oxide anchor because of the perfect alignment of all three of its donor groups for binding to inorganic surfaces. It can therefore be used in the design of organic linkers for m
