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1,2,4,6-Tetra-O-acetyl-3-chloro-3-deoxy-D-glucopyranose, with the CAS number 104013-04-9, is a white crystalline solid that serves as a valuable compound in the field of organic synthesis. It is a derivative of D-glucopyranose, a monosaccharide, where four hydroxyl groups are acetylated, and the third carbon is substituted with a chlorine atom, making it a versatile building block for various chemical reactions and applications.

104013-04-9

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104013-04-9 Usage

Uses

Used in Organic Synthesis:
1,2,4,6-Tetra-O-acetyl-3-chloro-3-deoxy-D-glucopyranose is used as a synthetic intermediate for the production of various complex organic compounds. Its unique structure allows for selective functionalization and modification, making it a valuable asset in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,2,4,6-Tetra-O-acetyl-3-chloro-3-deoxy-D-glucopyranose is used as a key building block for the development of novel drug candidates. Its structural diversity and reactivity enable the creation of new molecules with potential therapeutic properties, contributing to the advancement of drug discovery and development.
Used in Chemical Research:
1,2,4,6-Tetra-O-acetyl-3-chloro-3-deoxy-D-glucopyranose is also utilized in academic and industrial research settings as a model compound for studying various chemical reactions and mechanisms. Its unique properties make it an ideal candidate for exploring new synthetic routes, reaction conditions, and catalysts, further expanding the knowledge base in organic chemistry.
Used in Material Science:
In the field of material science, 1,2,4,6-Tetra-O-acetyl-3-chloro-3-deoxy-D-glucopyranose can be employed as a component in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its incorporation into polymers, coatings, or other materials can lead to innovative applications in various industries, including electronics, automotive, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 104013-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,1 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104013-04:
(8*1)+(7*0)+(6*4)+(5*0)+(4*1)+(3*3)+(2*0)+(1*4)=49
49 % 10 = 9
So 104013-04-9 is a valid CAS Registry Number.

104013-04-9SDS

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 [(2R,3R,4S,5S)-3,5,6-triacetyloxy-4-chlorooxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names 3-Chloro-3-deoxy-D-glucopyranose Tetraacetate

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:104013-04-9 SDS

104013-04-9Downstream Products

104013-04-9Relevant academic research and scientific papers

The synthesis and hydrolysis of a series of deoxy- and deoxyfluoro-α-D-"glucopyranosyl" phosphates

Withers, Stephen G.,Percival, M. David,Street, Ian P.

, p. 43 - 66 (2007/10/02)

The syntheses of three deoxy-α-D-"glucopyranosyl" phosphates and a series of dideoxymonofluoro- and dideoxydifluoro-α-D-glucopyranosyl phosphates are described.Rate constants for their acid-catalyzed hydrolysis were determined.Deoxygenation in the sugar r

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