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4-(2-HYDROXYETHYL)THIOMORPHOLINE 1,1-DIOXIDE, also known as VESTA COR, is a versatile chemical substance characterized by its unique structure that includes a morpholine ring, a thioether, and a dioxolane ring. This structure, along with the presence of a hydroxyl group, endows it with the ability to form hydrogen bonds, making it valuable for a range of chemical reactions and industrial applications. Its properties, such as boiling point, melting point, and flash point, are dependent on purity and other conditions, and it must be handled with care according to safety guidelines outlined in its Material Safety Data Sheet.

26475-62-7

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26475-62-7 Usage

Uses

Used in Chemical Reactions:
4-(2-HYDROXYETHYL)THIOMORPHOLINE 1,1-DIOXIDE is used as a reagent for its ability to form hydrogen bonds, facilitating specific chemical reactions that require such interactions.
Used in Industrial Applications:
In various industries, 4-(2-HYDROXYETHYL)THIOMORPHOLINE 1,1-DIOXIDE is used as a component in the production of different products due to its unique structural properties and reactivity.
Used in Pharmaceutical Industry:
4-(2-HYDROXYETHYL)THIOMORPHOLINE 1,1-DIOXIDE is used as an intermediate in the synthesis of pharmaceutical compounds, leveraging its chemical properties to contribute to the development of new drugs.
Used in Material Science:
4-(2-HYDROXYETHYL)THIOMORPHOLINE 1,1-DIOXIDE is used as a modifier or additive in material science to enhance the properties of various materials, such as improving solubility or stability.

Check Digit Verification of cas no

The CAS Registry Mumber 26475-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,7 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26475-62:
(7*2)+(6*6)+(5*4)+(4*7)+(3*5)+(2*6)+(1*2)=127
127 % 10 = 7
So 26475-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO3S/c8-4-1-7-2-5-11(9,10)6-3-7/h8H,1-6H2

26475-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,1-dioxo-1,4-thiazinan-4-yl)ethanol

1.2 Other means of identification

Product number -
Other names 4-(2-Hydroxyethyl)thiomorpholine 1,1-Dioxide

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:26475-62-7 SDS

26475-62-7Relevant academic research and scientific papers

Development of a Safe and High-Throughput Continuous Manufacturing Approach to 4-(2-Hydroxyethyl)thiomorpholine 1,1-Dioxide

Strotman, Neil A.,Tan, Yichen,Powers, Kyle W.,Soumeillant, Maxime,Leung, Simon W.

, p. 721 - 727 (2018)

Continuous processing enabled the highly energetic double conjugate addition of ethanolamine to divinylsulfone to prepare 2 kg of 4-(2-hydroxyethyl)thiomorpholine 1,1-dioxide, as an intermediate in the synthesis of HIV Maturation Inhibitor BMS-955176. In situ IR was employed to monitor the steady state of the transformation for increased robustness via appearance of the thiomorpholine dioxide moiety and disappearance of the divinylsulfone. Surprisingly, a series of oligomers formed as intermediates, which converted to product with extended aging or heating, consistent with computational predictions. By running this process in flow, the highly exothermic reaction could be safely executed in an equal volume of water as the only solvent, despite an adiabatic temperature rise of 142 °C, leading to a streamlined and efficient process.

C-3 NOVEL TRITERPENE WITH C-17 AMINE DERIVATIVES AS HIV INHIBITORS

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Page/Page column 24; 25, (2017/09/15)

The present invention relates to to C-3 novel triterpene with C-17 amine derivatives of formula (I); or pharmaceutically acceptable salts, solvates, hydrates, tautomers, stereoisomers, prodrugs, compositions or combination thereof, wherein R1, R2, R3, R4, R5 and 'n' are as defined herein. The present invention also relates to pharmaceutical compositions comprising compounds of formula (I) and process for preparing them, and their use for the treatment of viral diseases and particularly HIV mediated diseases.

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