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Pyridine, 4-[(2R,4S)-2-(4-nitrophenoxy)-2-oxido-1,3,2-dioxaphosphorinan-4-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

685111-88-0

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685111-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 685111-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,1,1 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 685111-88:
(8*6)+(7*8)+(6*5)+(5*1)+(4*1)+(3*1)+(2*8)+(1*8)=170
170 % 10 = 0
So 685111-88-0 is a valid CAS Registry Number.

685111-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-(4S)-trans-2-(4-nitrophenoxy)-2-oxido-4-(pyridin-4-yl)-1,3,2-dioxaphosphorinane

1.2 Other means of identification

Product number -
Other names trans-4-[(S)-pyridin-4-yl]-2-(4-nitrophenoxy)-2-oxo-1,3,2-dioxaphosphorinane

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:685111-88-0 SDS

685111-88-0Relevant academic research and scientific papers

Stereoselective synthesis of nucleoside monophosphate HepDirect prodrugs

Reddy, K. Raja,Boyer, Serge H.,Erion, Mark D.

, p. 4321 - 4324 (2005)

Synthesis of HepDirect prodrugs of nucleoside monophosphates via phosphorylation with a chiral reagent forms a new asymmetric center at phosphorus and produces two diastereomers. Coupling of chiral phosphoramidite 6 derived from (S)-diol 5 with ara-A foll

Compound for treating metabolic diseases as well as preparation method and application thereof

-

Paragraph 0098; 0148-0158, (2019/07/04)

The invention provides a compound for treating metabolic diseases, the compound has a structure represented by formula (I) or formula (II), or a racemate, a stereoisomer, a geometric isomer, a tautomer, a solvate, a hydrate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof. The compounds provided by the invention are FXR and/or TGR5 receptor activators, and the compounds havethe activity of activating FXR and/or TGR5 receptors, and can be used for preparing medicines for treating chronic liver diseases, metabolic diseases or portal hypertension.

Synthesis and characterization of a novel liver-targeted prodrug of cytosine-1-β-D-arabinofuranoside monophosphate for the treatment of hepatocellular carcinoma

Boyer, Serge H.,Sun, Zhili,Jiang, Hongjian,Esterbrook, Julie,Gómez-Galeno, Jorge E.,Craigo, William,Reddy, K. Raja,Ugarkar, Bheemarao G.,MacKenna, Deidre A.,Erion, Mark D.

, p. 7711 - 7720 (2007/10/03)

Cytotoxic nucleosides have proven to be ineffective for the treatment of hepatocellular carcinoma (HCC) due, in part, to their inadequate conversion to their active nucleoside triphosphates (NTP) in the liver tumor and high conversion in other tissues. Th

Novel 2'-C-methyl nucleoside derivatives

-

Page/Page column 49-50, (2008/06/13)

Compounds of Formula I, stereoisomers, and pharmaceutically acceptable salts or prodrugs thereof, their preparation, and their uses for the treatment of hepatitis C viral infection are described:

Novel cytarabine monophosphate prodrugs

-

Page/Page column 16-17, (2008/06/13)

Compounds of Formula I, their preparation and uses are described: wherein: M and V are cis to one another and MH is cytarabine; the 5′ oxygen of said cytarabine is attached to the phosphorus; V is 4-pyridyl; and pharmaceutically acceptable prodrugs and salts thereof.

Design, Synthesis, and Characterization of a Series of Cytochrome P 450 3A-Activated Prodrugs (HepDirect Prodrugs) Useful for Targeting Phosph(on)ate-Based Drugs to the Liver

Erion, Mark D.,Reddy, K. Raja,Boyer, Serge H.,Matelich, Michael C.,Gomez-Galeno, Jorge,Lemus, Robert H.,Ugarkar, Bheemarao G.,Colby, Timothy J.,Schanzer, Juergen,Van Poelje, Paul D.

, p. 5154 - 5163 (2007/10/03)

A new class of phosphate and phosphonate prodrugs, called HepDirect prodrugs, is described that combines properties of rapid liver cleavage with high plasma and tissue stability to achieve increased drug levels in the liver. The prodrugs are substituted c

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