320405-84-3 Usage
Uses
Used in Pharmaceutical Industry:
6-Hydroxy-5-nitronicotinonitrile is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form heterocyclic compounds, which are essential in the development of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
6-Hydroxy-5-nitronicotinonitrile is used as a building block in the synthesis of agrochemicals, contributing to the development of new compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Organic Chemistry:
6-Hydroxy-5-nitronicotinonitrile is used as a reagent in organic chemistry reactions, particularly for the formation of heterocyclic compounds, which are important in the synthesis of various organic compounds with diverse applications.
Used as a Chelating Agent:
6-Hydroxy-5-nitronicotinonitrile is used as a chelating agent for its ability to bind to metal ions such as copper and iron, which can be utilized in various industrial applications, including the development of metal complexes with specific properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 320405-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,4,0 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 320405-84:
(8*3)+(7*2)+(6*0)+(5*4)+(4*0)+(3*5)+(2*8)+(1*4)=93
93 % 10 = 3
So 320405-84-3 is a valid CAS Registry Number.
320405-84-3Relevant articles and documents
NEW ANTIBACTERIAL COMPOUNDS
-
, (2018/01/19)
The present invention relates to novel antibacterial compounds, pharmaceutical compositions containing them and their use as antimicrobials.
New tetracyclic 1,4-oxazepines constructed via practically simple tandem condensation strategy from readily available synthons
Sapegin, Alexander V.,Kalinin, Stanislav A.,Smirnov, Alexey V.,Dorogov, Mikhail V.,Krasavin, Mikhail
, p. 1077 - 1083 (2014/01/23)
A streamlined synthetic methodology towards novel tetracyclic 1,4-oxazepines from readily available precursors is described. The compounds, designed as more soluble version of the earlier described, poorly soluble dibenzo[b,f][1,4]oxazepines, were obtained in high yields and as a single regioisomer as a result of three tandem chemical events - nucleophilic aromatic substitution, Smiles rearrangement and denitrocyclization.
Imidazopyridinone derivatives and their use as phosphodiesterase inhibitors
-
, (2008/06/13)
A compound (Ia): wherein the variables are defined in the specification, its prodrug or a pharmaceutically acceptable salt thereof useful in the treatment of angina, hypertension etc.
