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2,3,4,6-Tetra-O-acetyl-β-D-galactose ethylxanthat is a chemical compound derived from β-D-galactose, a monosaccharide found in many carbohydrates. 2,3,4,6-Tetra-O-acetyl-β-D-galactose ethylxanthat is characterized by the presence of four acetyl groups attached to the hydroxyl groups of the galactose molecule, which enhances its reactivity and makes it suitable for various chemical reactions. The ethylxanthat group further contributes to the unique properties of the compound, rendering it valuable in the synthesis of advanced materials and pharmaceuticals. It also holds potential in the development of carbohydrate-based drugs and as a building block for constructing complex organic molecules, making it an important player in the field of organic chemistry with diverse applications across different industries.

29587-08-4

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29587-08-4 Usage

Uses

Used in Biochemistry:
2,3,4,6-Tetra-O-acetyl-β-D-galactose ethylxanthat is used as a reagent for the synthesis of complex organic molecules and in the development of carbohydrate-based drugs. Its unique structure and reactivity make it a valuable component in biochemical research and drug discovery.
Used in Organic Synthesis:
In the field of organic synthesis, 2,3,4,6-Tetra-O-acetyl-β-D-galactose ethylxanthat is used as a building block for creating advanced materials. Its versatile chemical properties allow for the formation of a wide range of compounds, making it an essential tool in the synthesis of novel materials with potential applications in various industries.
Used in Pharmaceutical Industry:
2,3,4,6-Tetra-O-acetyl-β-D-galactose ethylxanthat is used as a key intermediate in the synthesis of pharmaceuticals. Its role in the development of new drugs is significant, as it can be incorporated into the molecular structures of potential therapeutic agents, contributing to the advancement of medicine.
Used in Material Science:
In material science, 2,3,4,6-Tetra-O-acetyl-β-D-galactose ethylxanthat is used as a component in the development of new materials with unique properties. Its incorporation into material compositions can lead to the creation of innovative products with applications in various sectors, such as electronics, energy, and environmental protection.

Check Digit Verification of cas no

The CAS Registry Mumber 29587-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,8 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29587-08:
(7*2)+(6*9)+(5*5)+(4*8)+(3*7)+(2*0)+(1*8)=154
154 % 10 = 4
So 29587-08-4 is a valid CAS Registry Number.

29587-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-bis(acetyloxy)-2-[(acetyloxy)methyl]-6-[(ethoxycarbothioyl)sulfanyl] tetrahydro-2H-pyran-4-yl-acetate

1.2 Other means of identification

Product number -
Other names dithiocarbonic acid O-ethyl ester-S-(tetra-O-acetyl-β-D-glucopyranosyl ester)

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:29587-08-4 SDS

29587-08-4Relevant academic research and scientific papers

Method for synthesizing isopropyl-beta-D-thiogalactoside (IPTG)

-

Paragraph 0017; 0018; 0019, (2018/11/22)

The invention provides a method for synthesizing isopropyl-beta-D-thiogalactoside (IPTG) and belongs to the technical field of organic synthesis. The method comprises the following steps: taking a compound beta-D-galactose pentaacetate as a raw material, and reacting with potassium ethyl xanthate in the presence of a catalyst so as to obtain tetraacetyl galactose ethyl xanthate; reacting with 2-bromopropane under an alkaline condition, so as to obtain the isopropyl-beta-D-thiogalactoside (IPTG). According to the synthetic method, the beta-D-galactose pentaacetate, potassium ethyl xanthate and2-bromopropane are taken as main raw materials, 2-mercaptopropane which is extremely unpleasant in smell, easy to diffuse and high in toxicity used in the original method is replaced, and the harm tothe environment is effectively avoided. The raw materials used in the method disclosed by the invention are readily available, the operating process is simple and convenient, the reaction condition ismild, and the method is safe, controllable and high in yield.

A novel approach for the formation of carbon-nitrogen bonds: Azidation of alkyl radicals with sulfonyl azides

Ollivier,Renaud

, p. 4717 - 4727 (2007/10/03)

Two preparatively attractive methods for the azidation of alkyl radicals are described. Secondary and tertiary alkyl iodides and dithiocarbonates are easily converted into the corresponding azides, either by reaction with ethanesulfonyl azide in the prese

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