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901752

Sigma-Aldrich

N-(tert-Butyl)-4′-((6-iodo-4-oxo-2-propylquinazolin-3(4H)-yl)methyl)-[1,1′-biphenyl]-2-sulfonamide

Sinónimos:

Aryl halide chemistry informer library compound X15

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About This Item

Fórmula empírica (notación de Hill):
C28H30IN3O3S
Número de CAS:
145863-90-7
Peso molecular:
615.53
Número MDL:
MFCD31707685
Código UNSPSC:
12352111
NACRES:
NA.22

Formulario

powder

mp

239-243 °C

grupo funcional

amine
iodo

cadena SMILES

Ic1cc2c(cc1)NC(=CCC)N(C2=O)Cc3ccc(cc3)c4c(cccc4)[S](=O)(=O)NC(C)(C)C

InChI

1S/C28H30IN3O3S/c1-5-8-26-30-24-16-15-21(29)17-23(24)27(33)32(26)18-19-11-13-20(14-12-19)22-9-6-7-10-25(22)36(34,35)31-28(2,3)4/h6-17,30-31H,5,18H2,1-4H3

Clave InChI

FJYBBPNOASJSBG-UHFFFAOYSA-N

Categorías relacionadas

Aplicación

This product is Informer compound X15 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 analyse a reaction′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.

Precaución

Not fully tested.

Otras notas

Chemistry informer libraries: a chemoinformatics enabled approach to evaluate and advance synthetic methods, Chem. Sci., 2016, 7, 2604-2613

Nanomole-scale high-throughput chemistry for the synthesis of complex molecules

Aryl amination using ligand-free Ni(II) salts and photoredox catalysis

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Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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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
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
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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