7399-69-1 Usage
Description
N-(2-Hydroxyethyl)-3-nitrobenzaMide, a nitrobenzamide derivative with the molecular formula C8H8N2O4, is a chemical compound that features a hydroxyethyl group. It is widely recognized for its versatility in organic synthesis and its potential as a precursor for the synthesis of other functionalized nitrobenzamides.
Uses
Used in Pharmaceutical Industry:
N-(2-Hydroxyethyl)-3-nitrobenzaMide is utilized as a building block for the production of pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicine.
Used in Chemical Industry:
In the chemical industry, N-(2-Hydroxyethyl)-3-nitrobenzaMide serves as a crucial intermediate for the synthesis of dyes and other organic compounds. Its ability to be functionalized makes it a valuable asset in creating a diverse range of products.
Used as a Precursor in Organic Synthesis:
N-(2-Hydroxyethyl)-3-nitrobenzaMide is recognized for its potential as a precursor in the synthesis of other functionalized nitrobenzamides. This role highlights its importance in expanding the scope of organic chemistry and the creation of novel compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 7399-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7399-69:
(6*7)+(5*3)+(4*9)+(3*9)+(2*6)+(1*9)=141
141 % 10 = 1
So 7399-69-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O4/c12-5-4-10-9(13)7-2-1-3-8(6-7)11(14)15/h1-3,6,12H,4-5H2,(H,10,13)
7399-69-1Relevant articles and documents
Benzimidazolium-based receptors: Case of iodide-water cluster induced supramolecular chain and improved fluorometric binding of iodide involving alcoholic group
Ghosh, Kumaresh,Saha, Indrajit
, p. 57 - 65 (2013/06/26)
Benzimidazolium-based receptors 1 and 2 have been designed and synthesized. Anion binding studies reveal their selective fluorescence sensing of iodide in the excited state by exhibiting greater quenching of emission of anthracene. In the ground state, they prefer to bind bromide ion. Incorporation of alcoholic -OH in 2 leads to better performance over the receptor 1. The cyclooctameric structure as constituted by inclusion water and iodide interaction leads to ID-supramolecular chain with the structure 1 in the solid state. 1H NMR, UV-vis and fluorescence spectroscopic methods were adopted to study the anion binding behavior.
2-Benzamidoethyl group - A novel type of phosphate protecting group for oligonucleotide synthesis
Guzaev,Manoharan
, p. 783 - 791 (2007/10/03)
A number of 5′-O-(4,4′-dimethoxytrityl)thymidine N,N-diisopropylamino phosphoramidites protected at P(III) with derivatives of 2-benzamidoethanol were synthesized and incorporated into synthetic oligonucleotides. Depending on substitution patterns at the
N-[hydroxy(amino)alkyl]amides of amino(nitro)benzoic acids
Bagrov,Vasil'ev,Efimov,Kol'tsov
, p. 674 - 678 (2007/10/03)
2-Aminoethanol and 3-amino-1-propanol react with methyl 3-nitro-and 4-nitrobenzoates in boiling toluene to afford the corresponding ethyl N-(hydroxyalkyl)nitrobenzoates. The reaction of methyl 3-nitro-and 4-nitrobenzoates with bis(2-hydroxyethyl)amine yie
