468104-07-6 Usage
Description
(S)-1-(2-NITRO-BENZENESULFONYL)-PYRROLIDIN-3-YLAMINE, with the chemical formula C11H13N3O4S, is a sulfonamide derivative featuring a pyrrolidine group and a nitro group attached to the benzene ring. (S)-1-(2-NITRO-BENZENESULFONYL)-PYRROLIDIN-3-YLAMINE is significant in the field of medicinal and organic chemistry due to its potential applications in pharmaceuticals and agrochemicals synthesis, as well as its utility as an enzyme and receptor inhibitor in biological systems.
Uses
Used in Pharmaceutical Synthesis:
(S)-1-(2-NITRO-BENZENESULFONYL)-PYRROLIDIN-3-YLAMINE is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, (S)-1-(2-NITRO-BENZENESULFONYL)-PYRROLIDIN-3-YLAMINE serves as an intermediate for the creation of compounds with pesticidal or herbicidal properties, contributing to the development of more effective and targeted agrochemicals.
Used in Enzyme and Receptor Inhibition:
(S)-1-(2-NITRO-BENZENESULFONYL)-PYRROLIDIN-3-YLAMINE has shown potential as an inhibitor of certain enzymes and receptors in biological systems. This makes it a valuable tool in drug discovery and development, as it can be used to study and modulate the activity of these biological targets.
Used in the Synthesis of Heterocyclic Compounds:
The presence of the nitro group in (S)-1-(2-NITRO-BENZENESULFONYL)-PYRROLIDIN-3-YLAMINE makes it a potentially useful building block for the synthesis of various heterocyclic compounds, which are important in the development of new pharmaceuticals and other chemical products.
Overall, (S)-1-(2-NITRO-BENZENESULFONYL)-PYRROLIDIN-3-YLAMINE is an important chemical with diverse applications in the field of medicinal and organic chemistry, playing a crucial role in the development of new pharmaceuticals, agrochemicals, and other chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 468104-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,8,1,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 468104-07:
(8*4)+(7*6)+(6*8)+(5*1)+(4*0)+(3*4)+(2*0)+(1*7)=146
146 % 10 = 6
So 468104-07-6 is a valid CAS Registry Number.
468104-07-6Relevant articles and documents
Urotensin-II receptor antagonists: Synthesis and SAR of N-cyclic azaalkyl benzamides
Jin, Jian,An, Ming,Sapienza, Anthony,Aiyar, Nambi,Naselsky, Diane,Sarau, Henry M.,Foley, James J.,Salyers, Kevin L.,Knight, Steven D.,Keenan, Richard M.,Rivero, Ralph A.,Dhanak, Dashyant,Douglas, Stephen A.
scheme or table, p. 3950 - 3954 (2009/05/07)
SAR exploration of the central diamine, benzyl, and terminal aminoalkoxy regions of the N-cyclic azaalkyl benzamide series led to the identification of very potent human urotensin-II receptor antagonists such as 1a with a Ki of 4 nM. The synthesis and structure-activity relationships (SAR) of N-cyclic azaalkyl benzamides are described.
