122452-56-6 Usage
Uses
Used in Organic Synthesis:
N-succinimidyl-2,4-dimethoxy-3-(tributylstannyl)benzoate is used as a reagent in organic synthesis for conducting Stille coupling reactions, which are essential for forming carbon-carbon bonds in various chemical structures.
Used in Bioconjugation:
In the field of bioconjugation, N-succinimidyl-2,4-dimethoxy-3-(tributylstannyl)benzoate is used as a linker to attach the compound to biomolecules, such as proteins or nucleic acids, for applications in drug delivery and diagnostics.
Used in Drug Delivery Systems:
N-succinimidyl-2,4-dimethoxy-3-(tributylstannyl)benzoate is used as a component in drug delivery systems to enhance the targeting and efficacy of therapeutic agents. Its ability to be attached to biomolecules allows for the development of targeted drug delivery systems that can specifically deliver drugs to diseased cells or tissues.
Used in Diagnostics:
In the diagnostics industry, N-succinimidyl-2,4-dimethoxy-3-(tributylstannyl)benzoate is used as a component in the development of diagnostic tools and assays. Its ability to be attached to biomolecules enables the creation of highly specific diagnostic agents that can detect and monitor various diseases and conditions.
Used in Medical Research:
N-succinimidyl-2,4-dimethoxy-3-(tributylstannyl)benzoate is used as a research tool in medical research to study the interactions between biomolecules and develop new therapeutic strategies. Its versatility and ability to be attached to various biomolecules make it a valuable compound for exploring novel approaches in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 122452-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,5 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122452-56:
(8*1)+(7*2)+(6*2)+(5*4)+(4*5)+(3*2)+(2*5)+(1*6)=96
96 % 10 = 6
So 122452-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H12NO6.3C4H9.Sn/c1-18-8-3-4-9(10(7-8)19-2)13(17)20-14-11(15)5-6-12(14)16;3*1-3-4-2;/h3-4H,5-6H2,1-2H3;3*1,3-4H2,2H3;/rC25H39NO6Sn/c1-6-9-16-33(17-10-7-2,18-11-8-3)24-20(30-4)13-12-19(23(24)31-5)25(29)32-26-21(27)14-15-22(26)28/h12-13H,6-11,14-18H2,1-5H3
122452-56-6Relevant academic research and scientific papers
Radiohalogenation conjugate technology
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, (2008/06/13)
Compounds of the formulae, STR1 are provided where L is a linking group of the formula, STR2 is --Sn(n--C4 H9)3 or --Sn(CH3)3, HgCl or --N2+ ; R is hydrogen, methyl, mono-, di- or oligosaccharide; and R' is methyl. The compounds are site-specifically halogenated or radiohalogenated at the A group and coupled with macromolecules such as monoclonal antibodies, peptides or other proteins.
