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52645-73-5

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  • Factory Price API 99% ETHYL 2,3,4,6-TETRA-O-ACETYL-ALPHA-D-THIOGLUCOPYRANOSIDE 52645-73-5 GMP Manufacturer

    Cas No: 52645-73-5

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52645-73-5 Usage

Description

ETHYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE is a white crystalline solid that serves as a crucial reagent in the synthesis of glucosides. Its unique chemical structure allows for versatile applications across various industries.

Uses

Used in Pharmaceutical Industry:
ETHYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE is used as a key reagent for the preparation of glucosides, which are essential in the development of various pharmaceutical compounds. These glucosides can be utilized in the synthesis of drugs targeting specific diseases and conditions, making this compound a valuable asset in the pharmaceutical sector.
Used in Chemical Research:
As a white crystalline solid with distinct chemical properties, ETHYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE is also used in chemical research for studying the properties and reactions of glucosides. This helps researchers gain a deeper understanding of the underlying chemistry and potentially discover new applications for these compounds.
Used in Food Industry:
In the food industry, ETHYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE can be used as a reagent for the synthesis of glucosides that serve as additives or enhancers in the production of various food products. These glucosides can improve the taste, texture, or shelf life of the final product, making this compound an important tool in the food industry.
Used in Cosmetics Industry:
ETHYL 2,3,4,6-TETRA-O-ACETYL-1-THIO-BETA-D-GLUCOPYRANOSIDE is also used in the cosmetics industry for the preparation of glucosides that can be incorporated into skincare and beauty products. These glucosides may have moisturizing, anti-aging, or other beneficial properties, making this compound a valuable ingredient in the development of cosmetics.

Check Digit Verification of cas no

The CAS Registry Mumber 52645-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52645-73:
(7*5)+(6*2)+(5*6)+(4*4)+(3*5)+(2*7)+(1*3)=125
125 % 10 = 5
So 52645-73-5 is a valid CAS Registry Number.

52645-73-5SDS

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 O-Acetyl-ethyl-thio-D-glucopyranose

1.2 Other means of identification

Product number -
Other names Ethyl 2,3,4,6-Tetra-O-acetyl-Beta-D-thioglucopyranoside

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:52645-73-5 SDS

52645-73-5Relevant articles and documents

Concise Synthesis of 1-Thioalkyl Glycoside Donors by Reaction of Per-O-acetylated Sugars with Sodium Alkanethiolates under Solvent-Free Conditions

Feng, Guang-Jing,Luo, Tao,Guo, Yang-Fan,Liu, Chun-Yang,Dong, Hai

, p. 3638 - 3646 (2022/02/07)

A relatively green method for synthesizing 1-thioalkyl glycosides has been developed, where sodium alkanethiolates were used to react with per-O-acetylated sugars instead of odorous alkyl mercaptans in the presence of BF3·Et2O without the use of solvents under mild conditions. Furthermore, we found that 1,2-trans-β-thioglycosides can be converted into corresponding 1,2-cis-α-thioglycosides in the presence of trifluoromethanesulfonic acid in nonpolar solvents under mild conditions. This provides a simple and efficient new approach for synthesizing challenging 1,2-cis-α-thioglycosides.

Beta-D-glucose short-chain fatty acid ester compound as well as preparation method and application thereof

-

Paragraph 0033; 0057; 0059, (2021/04/03)

The invention discloses a beta-D-glucose short-chain fatty acid ester compound as well as a preparation method and application thereof, and belongs to the technical field of organic synthesis. The compound is a compound shown as a formula I, or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a prodrug of the compound shown as the formula I. The formula is as shown in the description, wherein R is a methyl group, an ethyl group, a propyl group, a propylene group, an isopropylidene group, a butyl group, a butylidene group, an isobutylidene group, an amyl group, a pentylidene group or an isoamylidene group. The compound has potential prevention and treatment effects on diabetes, hyperlipidemia, atherosclerosis, Alzheimer's disease, cardiovascular and cerebrovascular diseases,inflammation, tumors and depression.

Chemical glucosylation of pyridoxine

Bachmann, Thomas,Rychlik, Michael

supporting information, (2020/02/13)

The chemical synthesis of pyridoxine-5′-β-D-glucoside (5′-β-PNG) was investigated using various glucoside donors and promoters. Hereby, the combination of α4,3-O-isopropylidene pyridoxine, glucose vested with different leaving and protecting groups and the application of stoichiometric amounts of different promoters was examined with regards to the preparation of the twofold protected PNG. Best results were obtained with 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl fluoride and boron trifluoride etherate (2.0 eq.) as promoter at 0 °C (59%). The deprotection was accomplished stepwise with potassium/sodium hydroxide in acetonitrile/water followed by acid hydrolysis with formic acid resulting in the chemical synthesis of 5′-β-PNG.

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