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2-amino-9-(3-deoxy-3-fluoro-beta-D-xylofuranosyl)-3,9-dihydro-6H-purin-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2-Amino-9-((2R,3S,4R,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1H-purin-6(9H)-one

    Cas No: 125291-15-8

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  • 125291-15-8 Structure
  • Basic information

    1. Product Name: 2-amino-9-(3-deoxy-3-fluoro-beta-D-xylofuranosyl)-3,9-dihydro-6H-purin-6-one
    2. Synonyms: 6H-Purin-6-one, 2-amino-9-(3-deoxy-3-fluoro-.beta.-D-xylofuranosyl)-1,9-dihydro-; 6H-Purin-6-one, 2-amino-9-(3-deoxy-3-fluoro-beta-D-xylofuranosyl)-1,9-dihydro-
    3. CAS NO:125291-15-8
    4. Molecular Formula: C10H12FN5O4
    5. Molecular Weight: 285.2318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125291-15-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 726.1°C at 760 mmHg
    3. Flash Point: 392.9°C
    4. Appearance: N/A
    5. Density: 2.17g/cm3
    6. Vapor Pressure: 3.94E-22mmHg at 25°C
    7. Refractive Index: 1.876
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-amino-9-(3-deoxy-3-fluoro-beta-D-xylofuranosyl)-3,9-dihydro-6H-purin-6-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-amino-9-(3-deoxy-3-fluoro-beta-D-xylofuranosyl)-3,9-dihydro-6H-purin-6-one(125291-15-8)
    12. EPA Substance Registry System: 2-amino-9-(3-deoxy-3-fluoro-beta-D-xylofuranosyl)-3,9-dihydro-6H-purin-6-one(125291-15-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 125291-15-8(Hazardous Substances Data)

125291-15-8 Usage

Derived from

Purine nucleoside adenosine

Core Structure

2-amino-9H-purine-6-one

Side Chain

3-deoxy-3-fluoro-beta-D-xylofuranosyl attached at the 9th position

Applications

Potential use in pharmaceutical research and drug development

Specific Applications

Design of antiviral and anticancer agents

Value

Unique structure and properties make it a valuable target for further study and potential therapeutic use.

Check Digit Verification of cas no

The CAS Registry Mumber 125291-15-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,2,9 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125291-15:
(8*1)+(7*2)+(6*5)+(5*2)+(4*9)+(3*1)+(2*1)+(1*5)=108
108 % 10 = 8
So 125291-15-8 is a valid CAS Registry Number.

125291-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-9-[(2R,3S,4R,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one

1.2 Other means of identification

Product number -
Other names dF.b.XG

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:125291-15-8 SDS

125291-15-8Downstream Products

125291-15-8Relevant articles and documents

1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-xylofuranose. A versatile precursor for the synthesis of 3-deoxy-3-fluoro-β-D-xylofuranosyl nucleosides as potential antiviral agents

Gosselin,Puech,Genu-Dellac,Imbach

, p. 1 - 17 (2007/10/02)

The title compound has been synthesized from D-xylose for use in the preparation of 3-deoxy-3-fluoro-β-D-xylofuranosyl nucleoside analogues and their 2-deoxy derivatives, as exemplified in the guanine and thymine series. The title compound has been synthe

SYNTHESIS OF 9-(3-DEOXY- AND 2,3-DIDEOXY-3-FLUORO-β-D-XYLOFURANOSYL)GUANINES AS POTENTIAL ANTIVIRAL AGENTS

Puech, Frederic,Gosselin, Gilles,Imbach, Jean-Louis

, p. 3171 - 3174 (2007/10/02)

The first synthesis of the title compounds 8 and 10 was accomplished by a multi-step approach involving prior preparation of a suitably protected fluorosugar 6.

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