59283-75-9 Usage
Description
4-Hydroxylamino-2,6-dinitrotoluene is a member of the nitrotoluene class, specifically a 2,6-dinitrotoluene derivative with an additional hydroxylamino substituent at the 4th position. It is a chemical compound that has various applications across different industries due to its unique properties.
Uses
Used in Chemical Synthesis:
4-Hydroxylamino-2,6-dinitrotoluene is used as an intermediate in the synthesis of various chemical compounds, particularly those involving the nitro and hydroxylamino functional groups. Its ability to form meta-depside bonds makes it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Hydroxylamino-2,6-dinitrotoluene is used as a building block for the development of new drugs, especially those targeting specific diseases or conditions. Its unique structure allows for the design of novel therapeutic agents with potential applications in various medical fields.
Used in Explosives Industry:
4-Hydroxylamino-2,6-dinitrotoluene is also used in the explosives industry as a component in the formulation of certain types of explosives. Its nitro and hydroxylamino groups contribute to the compound's reactivity and energy release, making it a useful ingredient in the development of high-performance explosives.
Used in Environmental Applications:
In environmental applications, 4-Hydroxylamino-2,6-dinitrotoluene can be utilized for the remediation of contaminated sites, particularly those affected by nitroaromatic compounds. Its chemical properties enable it to interact with and neutralize harmful pollutants, thus playing a role in environmental cleanup efforts.
Used in Research and Development:
4-Hydroxylamino-2,6-dinitrotoluene is also used in research and development settings, where it serves as a model compound for studying the properties and reactivity of nitrotoluene derivatives. This helps scientists and researchers gain a better understanding of the underlying chemistry and develop new strategies for the synthesis and application of related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 59283-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,8 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59283-75:
(7*5)+(6*9)+(5*2)+(4*8)+(3*3)+(2*7)+(1*5)=159
159 % 10 = 9
So 59283-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O5/c1-4-6(9(12)13)2-5(8-11)3-7(4)10(14)15/h2-3,8,11H,1H3
59283-75-9Relevant articles and documents
Reductive transformation of bound trinitrophenyl residues and free TNT during a bioremediation process analyzed by immunoassay
Achtnich, Christof,Pfortner, Peter,Weller, Michael G.,Niessner, Reinhard,Lenke, Hiltrud,Knackmuss, Hans-Joachim
, p. 3421 - 3426 (1999)
To follow the fate of bound metabolites of TNT in soil, a synthetic trinitrophenyl residue covalently linked to humic acids was used as model compound. A selective monoclonal antibody was able to detect chemical changes of the nitro groups of the bound re
A comparative study of the structure, energetic performance and stability of nitro-NNO-azoxy substituted explosives
Wang, Yuan,Li, Shenghua,Li, Yuchuan,Zhang, Rubo,Wang, Dong,Pang, Siping
, p. 20806 - 20813 (2015/02/19)
2,4-Dinitro-NNO-azoxytoluene and 2,6-dinitro-4-nitro-NNO-azoxytoluene were synthesized as energetic compounds. Their structures and properties were studied by X-ray diffractometry, nuclear magnetic resonance and infrared spectroscopy. The differences betw
ANALYTE DETECTION
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, (2008/12/08)
The present invention relates to sensitive SE(R)RS based methods for detecting analytes such as explosives and drugs, which may be present in a sample at extremely low levels. The methods may be generally carried out in situ employing novel chemistry whic
Characteristic features of the selective action of platinum-doped glass fiber woven catalysts in the liquid-phase reduction of polyfunctional aromatic nitro compounds
Chuntiag, Wu,Dorokhov,Boiko,Bal'zhinimaev,Barelko
, p. 111 - 113 (2007/10/03)
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