901749
(R)-5-((1H-1,2,3-Triazol-1-yl)methyl)-3-(3-fluoro-4-iodophenyl)oxazolidin-2-one
Synonym(s):
Aryl halide chemistry informer library compound X14
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About This Item
Empirical Formula (Hill Notation):
C12H10FIN4O2
CAS Number:
Molecular Weight:
388.14
MDL number:
UNSPSC Code:
12352101
NACRES:
NA.22
Pricing and availability is not currently available.
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form
powder or crystals
mp
195-200 °C (w/ decomp.)
Application
This product is Informer compound X14 of the Aryl halide chemistry informer library developed by chemists at Merck & Co., Inc., Kenilworth, NJ, U.S., which contains 18 drug-like molecules representative of those encountered in complex synthesis. By screening a new reaction against the informer library, chemists can directly compare and analyze a reactions′s successes and shortcomings among different methods and various research teams. It may also be used to facilitate deeper method development for performance or utility.
Caution
Not fully tested.
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Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Nanomole-scale high-throughput chemistry for the synthesis of complex molecules.
Buitrago Santanilla, et al.
Science, 347, 49-53 (2015)
Emily B Corcoran et al.
Science (New York, N.Y.), 353(6296), 279-283 (2016-06-25)
Over the past two decades, there have been major developments in transition metal-catalyzed aminations of aryl halides to form anilines, a common structure found in drug agents, natural product isolates, and fine chemicals. Many of these approaches have enabled highly
Alexander Buitrago Santanilla et al.
Science (New York, N.Y.), 347(6217), 49-53 (2015-01-03)
At the forefront of new synthetic endeavors, such as drug discovery or natural product synthesis, large quantities of material are rarely available and timelines are tight. A miniaturized automation platform enabling high-throughput experimentation for synthetic route scouting to identify conditions
Peter S Kutchukian et al.
Chemical science, 7(4), 2604-2613 (2016-04-21)
Major new advances in synthetic chemistry methods are typically reported using simple, non-standardized reaction substrates, and reaction failures are rarely documented. This makes the evaluation and choice of a synthetic method difficult. We report a standardized complex molecule diagnostic approach
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