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Home/Compounds/Research Reagent/N-[9-[(2R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenyl-methoxy]methyl]-4-[2-cyanoethoxy-(diisopropylamino)phosphanyl]oxy-3,3-difluoro-tetrahydrofuran-2-yl]purin-6-yl]benzamide
C47H50F2N7O7P
893.9 g/mol
Research Reagent

N-[9-[(2R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenyl-methoxy]methyl]-4-[2-cyanoethoxy-(diisopropylamino)phosphanyl]oxy-3,3-difluoro-tetrahydrofuran-2-yl]purin-6-yl]benzamide

CAS3055573-22-0
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound

This compound is a research reagent for chemical biology, identified as a highly flexible molecule with a complex polycyclic structure. Its configuration is marked by stereochemical centers and includes functional groups such as an amide, ethers, and a nitrile, contributing to its use in laboratory investigations.

Research compound for chemical biology studies

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Referencesame scaffold

N-[9-[(2R,3R,4R,5R)-5-[(1R)-1-[bis(4-methoxyphenyl)-phenyl-methoxy]ethyl]-4-[2-cyanoethoxy-(diisopropylamino)phosphanyl]oxy-3-fluoro-tetrahydrofuran-2-yl]purin-6-yl]benzamide

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research compound

Referencesame scaffold

N-[9-[(2R,3R,4R,5R)-5-[(1R)-1-[bis(4-methoxyphenyl)-phenyl-methoxy]ethyl]-4-[2-cyanoethoxy-(diisopropylamino)phosphanyl]oxy-3-methoxy-tetrahydrofuran-2-yl]purin-6-yl]benzamide

CAS3055727-88-0

research compound

Referencesame scaffold

N-[9-[(2R,3R,4R,5R)-5-[(1S)-1-[bis(4-methoxyphenyl)-phenyl-methoxy]ethyl]-4-[2-cyanoethoxy-(diisopropylamino)phosphanyl]oxy-3-methoxy-tetrahydrofuran-2-yl]purin-6-yl]benzamide

CAS3060423-81-3

research compound

Identifiers
IUPAC Name

N-[9-[(2R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-3,3-difluorooxolan-2-yl]purin-6-yl]benzamide

InChIKey

QSNSJMVRIZTBGX-QVUJBPGYSA-N

SMILES

CC(C)N(C(C)C)P(OCCC#N)O[C@@H]1[C@H](O[C@H](C1(F)F)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC

Synonyms (1)

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