258834-81-0 Usage
Chemical structure
A complex molecule with multiple functional groups, including a 1,2-benzenediamine core, a tetrahydro-2,2-dimethyl-4H-1,3-dioxolo4,5-cpyrrol-4-yl moiety, N,N,N,N-tetrakis(4-methoxyphenyl)methyl substituents, and a 6-(1,1-dimethylethyl)dimethylsilyloxymethyl group.
Functional groups
The compound contains various functional groups, such as amines, ethers, and silyl ethers, which contribute to its reactivity and potential applications.
Stereochemistry
The compound has specific stereochemistry, with the 3aS, 4S, 6R, and 6aR configurations, which can influence its biological activity and interactions with other molecules.
Molecular weight
The molecular weight of the compound is relatively high due to its complex structure, which can affect its solubility, stability, and transport properties.
Potential applications
Given its complex structure and multiple functional groups, the compound may have potential applications in various fields, including pharmaceuticals, materials science, and organic synthesis.
Reactivity
The compound's reactivity may be influenced by its functional groups, stereochemistry, and molecular weight, making it a candidate for further study and potential use in chemical reactions and processes.
Stability
The stability of the compound may be affected by factors such as temperature, pH, and the presence of other reactive species, which could impact its shelf life and handling requirements.
Solubility
The compound's solubility in various solvents may be influenced by its functional groups, molecular weight, and stereochemistry, which could affect its formulation and administration in potential applications.
Biological activity
The compound's complex structure and multiple functional groups may contribute to its potential biological activity, making it a candidate for further study in the context of drug discovery and development.
Synthesis
The synthesis of this complex compound may involve multiple steps and require careful control of reaction conditions to achieve the desired stereochemistry and functional group incorporation.
Check Digit Verification of cas no
The CAS Registry Mumber 258834-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,8,8,3 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 258834-81:
(8*2)+(7*5)+(6*8)+(5*8)+(4*3)+(3*4)+(2*8)+(1*1)=180
180 % 10 = 0
So 258834-81-0 is a valid CAS Registry Number.
258834-81-0Relevant articles and documents
Transition state analogue inhibitors of protozoan nucleoside hydrolases
Furneaux, Richard H.,Schramm, Vern L.,Tyler, Peter C.
, p. 2599 - 2606 (2007/10/03)
Protozoan parasites are unable to synthesize purines de novo and must rely on purine salvage pathways for their requirements. Nucleoside hydrolases, which are not found in mammals, function as key enzymes in purine salvage in protozoa. Inhibition of these enzymes may disrupt purine supply and specific inhibitors are potential therapeutic agents for the control of protozoan infections. A series of 1,4-dideoxy-1,4-imino-D-ribitols bearing C- bonded aromatic substituents at C-1 have been synthesized, following carbanion additions to the imine 2, and tested as potential nucleoside hydrolase inhibitors. Nucleoside analogues 8, 11, 14, 17, 20, 24-26, 28 exhibit K(i) values in the range 0.2-22 μM against two representative isozymes of protozoan nucleoside hydrolases. (C) 1999 Elsevier Science Ltd.
