92511-12-1 Usage
Description
TERT-BUTYL(4-IODOBUTOXY)DIMETHYLSILANE is a chemical compound that serves as a reagent in the multi-step synthesis of spermine synthon and decanucleotide-spermine conjugates. It is characterized by its unique structure, which includes a tert-butyl group, an iodobutoxy group, and two dimethylsilanes.
Uses
Used in Pharmaceutical Industry:
TERT-BUTYL(4-IODOBUTOXY)DIMETHYLSILANE is used as a reagent for the synthesis of spermine synthon and decanucleotide-spermine conjugates, which are important in the development of pharmaceutical compounds. Its role in the synthesis process is crucial for the production of these conjugates, which have potential applications in various therapeutic areas.
In the synthesis of spermine synthon, TERT-BUTYL(4-IODOBUTOXY)DIMETHYLSILANE acts as a key intermediate, facilitating the formation of the desired product. TERT-BUTYL(4-IODOBUTOXY)DIMETHYLSILANE is essential for the subsequent synthesis of decanucleotide-spermine conjugates, which are used in the development of targeted drug delivery systems and other pharmaceutical applications.
Overall, TERT-BUTYL(4-IODOBUTOXY)DIMETHYLSILANE plays a significant role in the pharmaceutical industry, particularly in the synthesis of compounds with potential therapeutic applications. Its unique properties and reactivity make it a valuable component in the development of new drugs and drug delivery systems.
Check Digit Verification of cas no
The CAS Registry Mumber 92511-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,1 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92511-12:
(7*9)+(6*2)+(5*5)+(4*1)+(3*1)+(2*1)+(1*2)=111
111 % 10 = 1
So 92511-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H23IOSi/c1-10(2,3)13(4,5)12-9-7-6-8-11/h6-9H2,1-5H3
92511-12-1Relevant articles and documents
Synthesis of seven-membered oxacycles. Part 2: The furan approach
Fall, Yagamare,Vidal, Beatriz,Alonso, David,Gómez, Generosa
, p. 4467 - 4469 (2003)
We describe an efficient new approach for the synthesis of seven-membered oxacycles that is based on the oxidation of a furan ring with singlet oxygen followed by an intramolecular Michael addition.
NUCLEIC ACID-POLYPEPTIDE COMPOSITIONS AND USES THEREOF
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Paragraph 0358, (2020/12/29)
Disclosed herein are compositions and pharmaceutical formulations that comprise a binding moiety conjugated to a modified polynucleic acid molecule and a polymer. Also described herein include methods for treating a cancer which utilize a composition or a
Platinum-catalyzed α,β-unsaturated carbene formation in the formal syntheses of frondosin B and liphagal
Huynh, Khoi Q.,Seizert, Curtis A.,Ozumerzifon, Tarik J.,Allegretti, Paul A.,Ferreira, Eric M.
supporting information, p. 294 - 297 (2017/11/28)
Formal syntheses of tetracyclic terpenoids frondosin B and liphagal are described. Both synthetic routes rely on the use of platinum-catalyzed α,β-unsaturated carbene formation for the key C-C bond forming transformations. The successful route toward frondosin B utilizes a formal (4 + 3) cycloaddition, while the liphagal synthesis features the vinylogous addition of an enol nucleophile as a key step. Both synthetic routes are discussed, revealing insights into structural requirements in the catalytic a,β-unsaturated carbene reaction manifold.
