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1-(2,3,5-Tribenzoyl--D-ribofuranosyl)-5-nitropyridine-2(1H)-one is a complex chemical compound characterized by its unique molecular structure. It features a nitro group, a pyridine ring, and a ribofuranosyl sugar moiety, with three benzoyl groups attached to the ribofuranosyl unit. As a synthetic compound, it holds potential for various applications in pharmaceutical research and drug development, although further investigation is necessary to determine its specific properties and uses.

59892-37-4

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59892-37-4 Usage

Uses

Used in Pharmaceutical Research:
1-(2,3,5-Tribenzoyl--D-ribofuranosyl)-5-nitropyridine-2(1H)-one is used as a research compound for exploring its potential in the development of new pharmaceutical agents. Its unique structure and functional groups may offer novel interactions with biological targets, potentially leading to the discovery of new therapeutics.
Used in Drug Development:
In the drug development industry, 1-(2,3,5-Tribenzoyl--D-ribofuranosyl)-5-nitropyridine-2(1H)-one is used as a lead compound for the design and synthesis of new drugs. Its complex structure may provide a foundation for the creation of molecules with specific biological activities, targeting various diseases and conditions.
Used in Chemical Synthesis:
1-(2,3,5-Tribenzoyl--D-ribofuranosyl)-5-nitropyridine-2(1H)-one is utilized as a synthetic building block in the chemical synthesis of more complex molecules. Its versatile structure allows for further functionalization and modification, enabling the development of a diverse range of chemical products with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 59892-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,9 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59892-37:
(7*5)+(6*9)+(5*8)+(4*9)+(3*2)+(2*3)+(1*7)=184
184 % 10 = 4
So 59892-37-4 is a valid CAS Registry Number.

59892-37-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-nitropyridin-2-one

1.2 Other means of identification

Product number -
Other names 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-5-nitropyridine-2(1H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59892-37-4 SDS

59892-37-4Relevant academic research and scientific papers

Synthesis of N3,5′-cyclo-4-(β-D-ribofuranosyl)-vic- triazolo[4,5-b]pyridin-5-one and its 3′-deoxysugar analogue as potential anti-hepatitis C virus agents

Wang, Peiyuan,Hollecker, Laurent,Pankiewicz, Krzysztof W.,Patterson, Steven E.,Whitaker, Tony,McBrayer, Tamara R.,Tharnish, Phillip M.,Stuyver, Lieven J.,Schinazi, Raymond F.,Otto, Michael J.,Watanabe, Kyoichi A.

, p. 957 - 960 (2007/10/03)

We recently discovered a novel compound, identified as N 3,5′-cyclo-4-(β-D-ribofuranosyl)-vic-triazolo[4,5-b] pyridinin-5-one, with anti-hepatitis C virus (HCV) activity in vitro. The structure was confirmed by chemical synthesis from 2-hydroxy

Synthesis of N3,5′-cyclo-4-(β-D-ribofuranosyl)-vic- triazolo[4,5-b]pyridin-5-one, a novel compound with anti-hepatitis C virus activity

Wang, Peiyuan,Hollecker, Laurent,Pankiewicz, Krzysztof W.,Patterson, Steven E.,Whitaker, Tony,McBrayer, Tamara R.,Tharnish, Phillip M.,Sidwell, Robert W.,Stuyver, Lieven J.,Otto, Michael J.,Schinazi, Raymond F.,Watanabe, Kyoichi A.

, p. 6100 - 6103 (2007/10/03)

A novel anti-hepatitis C virus (HCV) agent, N3,5′-cyclo-4- (β-D-ribofuranosyl)-vic-triazolo(4,5-b]pyridinin-5-one, was identified, and the structure was confirmed by chemical synthesis from 2-hydroxy-5- nitropyridine.

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