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29218-07-3

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  • 4-Fluoro-4-deoxy-D-glucopyranose CAS NO.29218-07-3 CAS NO.29218-07-3

    Cas No: 29218-07-3

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29218-07-3 Usage

Description

4-FLUORO-4-DEOXY-D-GLUCOPYRANOSE, also known as 4-Deoxy-4-fluoro-D-glucose (CAS# 29218-07-3), is a white crystalline solid compound that is useful in organic synthesis. It is a modified form of D-glucose, a naturally occurring sugar, with a fluorine atom replacing one of the hydroxyl groups, which may alter its chemical properties and reactivity.

Uses

Used in Organic Synthesis:
4-FLUORO-4-DEOXY-D-GLUCOPYRANOSE is used as a synthetic building block for the creation of various complex organic molecules. Its unique structure, with the fluorine atom substitution, makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-FLUORO-4-DEOXY-D-GLUCOPYRANOSE is used as a key intermediate in the development of novel drug candidates. Its unique chemical properties allow for the design of molecules with specific biological activities, potentially leading to the discovery of new therapeutic agents.
Used in Research and Development:
4-FLUORO-4-DEOXY-D-GLUCOPYRANOSE is also utilized in research and development settings, where it can be employed to study the effects of sugar modifications on biological systems. This can help researchers understand the role of sugars in various biological processes and may contribute to the development of new diagnostic tools or therapeutic strategies.
Used in Material Science:
In material science, 4-FLUORO-4-DEOXY-D-GLUCOPYRANOSE may be used to develop new materials with specific properties, such as improved stability or reactivity. Its unique structure could be exploited to create materials with enhanced performance in various applications, including energy storage, catalysis, or environmental remediation.
Overall, 4-FLUORO-4-DEOXY-D-GLUCOPYRANOSE is a versatile compound with a wide range of potential applications across different industries, thanks to its unique chemical properties and its role as a synthetic building block.

Check Digit Verification of cas no

The CAS Registry Mumber 29218-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,1 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29218-07:
(7*2)+(6*9)+(5*2)+(4*1)+(3*8)+(2*0)+(1*7)=113
113 % 10 = 3
So 29218-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11FO5/c7-3-2(1-8)12-6(11)5(10)4(3)9/h2-6,8-11H,1H2

29218-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Deoxy-4-fluoro-D-glucose

1.2 Other means of identification

Product number -
Other names 4-FLUORO-4-DEOXY-D-GLUCOPYRANOSE

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:29218-07-3 SDS

29218-07-3Relevant articles and documents

SYNTHESIS OF 3-DEOXY-3-FLUORO-D-MANNOSE AND 4-DEOXY-4-FLUORO-D-MANNOSE

Rasmussen, James R.,Tafuri, Sherrie R.,Smale, Stephen T.

, p. 21 - 30 (2007/10/02)

Addition of potassium cyanide to 2-deoxy-2-fluoro-D-arabinose (1) at pH 7.8 followed by catalytic hydrogenation over palladium-barium sulfate (5percent) produced 3-deoxy-3-fluoro-D-glucose (4) and 3-deoxy-3-fluoro-D-mannose (5) in 25 and 40 percent isolated yields, respectively.The epimeric sugars were purified by passage through a column of Dowex-50W x 8 (Ca2+).In a similar manner, 3-deoxy-3-fluoro-D-arabinose (6) was converted into 4-deoxy-4-fluoro-D-glucose (9) and 4-deoxy-4-fluoro-D-mannose (10) in 27 and 45 percent isolated yields, respectively.Deoxyfluorohexoses 4,5,9 and 10 enriched with carbon-13 and crbon-14 at C-1 have been prepared by this procedure.

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