620161-75-3 Usage
Description
Carbonic acid 2-tert-butoxycarbonyloxyMethyl-allyl ester tert-butyl ester is a complex chemical compound derived from carbonic acid, characterized by the presence of a carbonic acid functional group along with tert-butoxycarbonyloxyMethyl-allyl and tert-butyl ester groups. carbonic acid 2-tert-butoxycarbonyloxyMethyl-allyl ester tert-butyl ester is likely utilized as a reagent or intermediate in various chemical reactions, particularly in the synthesis of pharmaceuticals and other organic compounds.
Uses
Used in Pharmaceutical Industry:
Carbonic acid 2-tert-butoxycarbonyloxyMethyl-allyl ester tert-butyl ester is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the tert-butoxycarbonyloxyMethyl-allyl and tert-butyl ester groups, allows for versatile reactions and the formation of diverse drug molecules.
Used in Organic Synthesis:
In the field of organic synthesis, carbonic acid 2-tert-butoxycarbonyloxyMethyl-allyl ester tert-butyl ester serves as a valuable reagent. Its functional groups enable a range of reactions, such as esterification, transesterification, and other condensation reactions, contributing to the synthesis of complex organic molecules.
Used in Chemical Research:
Carbonic acid 2-tert-butoxycarbonyloxyMethyl-allyl ester tert-butyl ester is also employed in chemical research to explore its properties and potential applications. Further studies and analysis are required to determine its specific characteristics, reactivity, and suitability for various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 620161-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 620161-75:
(8*6)+(7*2)+(6*0)+(5*1)+(4*6)+(3*1)+(2*7)+(1*5)=113
113 % 10 = 3
So 620161-75-3 is a valid CAS Registry Number.
620161-75-3Relevant articles and documents
Successive Nucleophilic and Electrophilic Allylation for the Catalytic Enantioselective Synthesis of 2,4-Disubstituted Pyrrolidines
Luo, Guoshun,Xiang, Ming,Krische, Michael J.
, p. 2493 - 2497 (2019)
Successive nucleophilic and electrophilic allylation mediated by the bis-Boc-carbonate derived from 2-methylene-1,3-propane diol enables formation of enantiomerically enriched 2,4-disubstituted pyrrolidines. An initial enantioselective iridium-catalyzed t
Assembly of Terpenoid Cores by a Simple, Tunable Strategy
Lahtigui, Ouidad,Emmetiere, Fabien,Zhang, Wei,Jirmo, Liban,Toledo-Roy, Samira,Hershberger, John C.,Macho, Jocelyn M.,Grenning, Alexander J.
supporting information, p. 15792 - 15796 (2016/12/16)
Oxygenated, polycyclic terpenoid natural products have important biological activities. Although total synthesis of such terpenes is widely studied, synthetic strategies that allow for controlled placement of oxygen atoms and other functionality remains a challenge. Herein, we present a simple, scalable, and tunable synthetic strategy to assemble terpenoid-like polycycloalkanes from cycloalkanones, malononitrile, and allylic electrophiles, abundantly available reagent classes.
6,11-3c-bicyclic 8a-azalide derivatives
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Page/Page column 30, (2009/06/27)
Compounds of Formula (I), and pharmaceutically acceptable salts, esters, and prodrugs thereof: (I) are disclosed, wherein A, B, D, L, X, Y, Z and R2′, are described herein. The compounds exhibit antibacterial properties. The compounds of Formul
