7H-Pyrrolo[2,3-d]pyrimidine-5-methanol, 4-chloro-7-[2-deoxy-3,5-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-beta-D-erythro-pentofuranosyl]-2-[[(1,1-dimethylethyl)dimethylsilyl]amino]-

97%

Reagent Code: #194704
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CAS Number 1200461-84-2

science Other reagents with same CAS 1200461-84-2

blur_circular Chemical Specifications

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Weight 657.51 g/mol
Formula C₃₀H₅₇ClN₄O₄Si₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of antiviral agents, particularly in the development of nucleoside analogs targeting RNA viruses. Its protected functional groups allow selective modification during multi-step synthesis, making it valuable in medicinal chemistry for constructing complex nucleoside structures. Commonly employed in research settings to prepare compounds with potential activity against hepatitis C, coronaviruses, and other viral pathogens. The silyl protecting groups enhance solubility in organic solvents and improve reaction yields during coupling steps.

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inventory 25mg
10-20 days ฿18,670.00

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7H-Pyrrolo[2,3-d]pyrimidine-5-methanol, 4-chloro-7-[2-deoxy-3,5-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-beta-D-erythro-pentofuranosyl]-2-[[(1,1-dimethylethyl)dimethylsilyl]amino]-
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Used as an intermediate in the synthesis of antiviral agents, particularly in the development of nucleoside analogs targeting RNA viruses. Its protected functional groups allow selective modification during multi-step synthesis, making it valuable in medicinal chemistry for constructing complex nucleoside structures. Commonly employed in research settings to prepare compounds with potential activity against hepatitis C, coronaviruses, and other viral pathogens. The silyl protecting groups enhance solubil

Used as an intermediate in the synthesis of antiviral agents, particularly in the development of nucleoside analogs targeting RNA viruses. Its protected functional groups allow selective modification during multi-step synthesis, making it valuable in medicinal chemistry for constructing complex nucleoside structures. Commonly employed in research settings to prepare compounds with potential activity against hepatitis C, coronaviruses, and other viral pathogens. The silyl protecting groups enhance solubility in organic solvents and improve reaction yields during coupling steps.

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