88-82-4 Usage
Description
2,3,5-Triiodobenzoic acid is an organic compound characterized by the presence of three iodine atoms attached to a benzoic acid structure. It exhibits unique chemical properties due to its polar nature and the presence of iodine atoms, which contribute to its diverse applications in various fields.
Uses
Used in Plant Biology Research:
2,3,5-Triiodobenzoic acid is used as a polar auxin transport inhibitor for studying the effects of auxin transport on plant growth and development. It helps researchers understand the role of auxins in plant physiology by inhibiting their transport and promoting endoreduplication in hypocotyls and cotyledons.
Used in Pharmaceutical Industry:
2,3,5-Triiodobenzoic acid is used as an active pharmaceutical ingredient for the development of drugs targeting various medical conditions. Its unique chemical properties make it a promising candidate for drug discovery and design, potentially leading to the creation of novel therapeutic agents.
Used in Chemical Synthesis:
2,3,5-Triiodobenzoic acid is used as a key intermediate in the synthesis of various organic compounds and materials. Its reactivity and functional groups make it a valuable building block for the production of specialty chemicals, dyes, and other industrial products.
Used in Analytical Chemistry:
2,3,5-Triiodobenzoic acid is used as a reference compound or analytical standard in various analytical techniques, such as chromatography, spectroscopy, and titration. Its distinct chemical properties allow for accurate measurements and comparisons in research and quality control applications.
Biochem/physiol Actions
2,3,5-Triiodobenzoic acid (TIBA) inhibits the translocation of indole-3-acetic acid transport.TIBA inhibits the colonization of the main root cortex by Laccaria bicolor S238 N and the formation of the Hartig net.
Check Digit Verification of cas no
The CAS Registry Mumber 88-82-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88-82:
(4*8)+(3*8)+(2*8)+(1*2)=74
74 % 10 = 4
So 88-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3I3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)/p-1
88-82-4Relevant articles and documents
X-ray contrast agent
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, (2008/06/13)
The present invention refers to a phospholipid-based compound, that is a phospholipid to which an X-ray contrast-giving moiety has been covalently linked, liposomes comprising said compound as well as the use of said liposomes as a diagnostic or contrast agent.
Compositions of iodobenzoic acid derivatives and cellulose derivatives for visualization of the gastrointestinal tract
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, (2008/06/13)
Disclosed are x-ray contrast compositions for oral or retrograde examination of the gastrointestinal tract comprising an x-ray producing agent of the formula or a pharmaceutically acceptable salt thereof STR1 wherein Z is H, halo, C1 -C20 alkyl, cycloalkyl, lower alkoxy, cyano, where the alkyl and cycloalkyl groups can be substituted with halogen or halo-lower-alkyl groups; R is C1 -C25 alkyl, cycloalkyl, or halo-lower-alkyl, each of which may be optionally substituted with halo, fluoro-lower-alkyl, aryl, lower-alkoxy, hydroxy, carboxy, lower-alkoxy carbonyl or lower-alkoxy-carbonyloxy; (CR1 R2)p -- (CR3 =CR4)m Q, or (CR1 R2)p -- C=C--Q; R1, R2, R3 and R4 are independently lower-alkyl, optionally substituted with halo; x is 1--3 y is 1--4; n is 1--5; m is 1--15; p is 1--10; and Q is H, lower-alkyl, lower-alkenyl, lower-alkynyl, lower-alkylene, aryl, or aryl-lower alkyl in a pharmaceutically acceptable carrier comprising a cellulose derivative.
Pesticide-polymer systems prepared from vinyl monomers
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, (2008/06/13)
Controlled release pesticide-polymer systems are prepared by the polymerization of vinyl monomers containing pendant pesticides. The vinyl monomers are prepared by reacting an acrylic acid derivative with a pesticide or a pesticide derivative having an active hydrogen. The pesticide-polymer systems prepared from the pesticide vinyl monomers release the active pesticide material by hydrolysis or chemical depolymerization under conditions of use.