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120-89-8

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120-89-8 Usage

Description

Parabanic acid, an imidazolidinone derivative, is a white crystalline solid with the chemical structure of imidazolidine substituted by oxo groups at positions 2, 4, and 5. It is recognized for its significance as a marker of free radical reactions in biological systems.

Uses

1. Used in Medical Applications:
Parabanic acid is used as a marker for monitoring free radical activity in vivo. This application aids in evaluating the effectiveness of pharmacological therapies involving radical scavengers, which are crucial for understanding and managing various diseases and conditions related to oxidative stress.
2. Used in Chemical Synthesis:
Parabanic acid serves as a valuable synthetic intermediate in the creation of various chemical compounds. Its versatile structure allows it to be a key component in the synthesis of numerous derivatives and complexes.
a. Used in Enantiospecific Assembly:
Parabanic acid is used as a reactant for the enantiospecific assembly of homochiral, hexanuclear palladium complexes. These complexes have potential applications in catalysis and other areas of chemistry.
b. Used in Mitsunobu Reactions:
It is also utilized in Mitsunobu reactions, which are a class of chemical reactions that involve the inversion of stereochemistry and the formation of new carbon-heteroatom bonds.
c. Used in Quantitative Cascade Condensation Reactions:
Parabanic acid is employed in quantitative cascade condensation reactions, which are multi-step processes that result in the formation of complex molecular structures.
d. Reactant for Synthesis of Pyridine Derivatives:
It is used as a reactant in the synthesis of pyridine derivatives, which are important compounds in the field of organic chemistry and have various applications, including pharmaceuticals and agrochemicals.
e. Reactant for Synthesis of Nitroesters:
Parabanic acid is used in the synthesis of nitroesters, which are compounds that find use in the production of explosives, propellants, and other industrial applications.
f. Reactant for Synthesis of Parabanic Acid Derivatives:
It is also used as a reactant for the synthesis of its own derivatives, which can have specialized applications in various fields, depending on their specific properties and structures.

Check Digit Verification of cas no

The CAS Registry Mumber 120-89-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120-89:
(5*1)+(4*2)+(3*0)+(2*8)+(1*9)=38
38 % 10 = 8
So 120-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H2N2O3/c6-1-2(7)5-3(8)4-1/h(H2,4,5,6,7,8)

120-89-8 Well-known Company Product Price

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  • Aldrich

  • (P209)  Parabanicacid  99%

  • 120-89-8

  • P209-5G-A

  • 1,745.64CNY

  • Detail

120-89-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name parabanic acid

1.2 Other means of identification

Product number -
Other names Parabanic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120-89-8 SDS

120-89-8Related news

Regular paperInfluence of solution acidity on the adsorption and charge transfer kinetics of PARABANIC ACID (cas 120-89-8) reduction09/03/2019

Parabanic acid reduction has been studied in the − 1.4 ⩽ H0 ⩽ 0.9 acidity range by the ac impedance technique. Changes in the adsorption of reactant and products with solution acidity lead to protonation equilibrium constants that differ from their bulk values. The observed pKa shifts were consi...detailed

Oxidative adsorption and hydrogen-mediated desorption of PARABANIC ACID (cas 120-89-8) on Pt(111) electrodes09/01/2019

The adsorption properties of parabanic acid (PBA) on Pt(111) electrodes are described. The process takes place with charge transfer at potentials higher than 0.175 V. The PBA adlayer is particularly stable against oxidation or CO adsorption but is desorbed upon hydrogen adsorption. Comparison be...detailed

[(η5-C5H5)Fe(CO)2](Fp)-complexes of the PARABANIC ACID (cas 120-89-8) mono- and dianion: synthesis, X-ray structures and reactivity of the heterocyclic ligand08/31/2019

[(η5-C5H5)Fe(CO)2](Fp)-complexes of the parabanic acid mono- and dianion have been synthesised in a photochemical reaction of FpI with parabanic acid and diisopropylamine in benzene. The former contains a reactive N(3)–H bond and can be readily thallated with TlOEt. Reaction of the thallated c...detailed

Experimental and theoretical investigation of the PARABANIC ACID (cas 120-89-8) molecule following VUV excitation and photodissociation08/29/2019

Photodissociation experiments have been performed for the parabanic acid (C3H2N2O3) molecule in vapor phase using time-of-flight mass spectrometry and synchrotron radiation in the VUV photon energy range. Electron ion coincidence (PEPICO) spectra and partial ion yields have been recorded as a fu...detailed

120-89-8Relevant articles and documents

Gas-solid reactions of single crystals: A study of reactions of NH 3 and NO2 with single crystalline organic substrates by infrared microspectroscopy

Jenkins, Samantha L.,Almond, Matthew J.,Atkinson, Samantha D.M.,Hollins, Peter,Knowles, John P.

, p. 1131 - 1139 (2005)

Reaction of single crystals of benzoic and trans-cinnamic acids with 200 Torr pressure of ammonia gas in a sealed glass bulb at 20 °C generates the corresponding ammonium salts; there is no sign of any 1:2 adduct as has been reported previously for related systems. Isotopic substitution using ND 3 has been used to aid identification of the products. Adipic acid likewise reacts with NH3 gas to form a product in which ammonium salts are formed at both carboxylic acid groups. Reaction of 0.5 Torr pressure of NO2 gas with single crystals of 9-methylanthracene and 9-anthracenemethanol in a flow system generates nitrated products where the nitro group appears to be attached at the 10-position, i.e. the position trans to the methyl or methoxy substituent on the central ring. Isotopic substitution using 15NO2 has been used to confirm the identity of the bands arising from the coordinated NO2 group. The products formed when single crystals of hydantoin are reacted with NO2 gas under similar conditions depend on the temperature of the reaction. At 20 °C, a nitrated product is formed, but at 65 °C this gives way to a product containing no nitro groups. The findings show the general applicability of infrared microspectroscopy to a study of gas-solid reactions of organic single crystals.

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Silica Metal Oxide Vesicles Catalyze Comprehensive Prebiotic Chemistry

Mattia Bizzarri, Bruno,Botta, Lorenzo,Pérez-Valverde, Maritza Iveth,Saladino, Raffaele,Di Mauro, Ernesto,García-Ruiz, Juan Manuel

, p. 8126 - 8132 (2018/05/29)

It has recently been demonstrated that mineral self-assembled structures catalyzing prebiotic chemical reactions may form in natural waters derived from serpentinization, a geological process widespread in the early stages of Earth-like planets. We have s

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