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CAS

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107825-27-4

Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-, is a chemical compound characterized by the molecular formula C13H15FNO2S. It is a thioether derivative featuring a fluorophenyl and morpholinyl substituent, which endows it with unique structural properties. As a potential drug agent, it has demonstrated promising biological activities in preclinical studies, positioning it as a candidate for further research and development within the pharmaceutical industry.

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  • 107825-27-4 Structure

  • Basic information

    1. Product Name: Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-
    2. Synonyms: Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-;2-(4-fluorophenyl)-1-(4-morpholinyl)Ethanethione
    3. CAS NO:107825-27-4
    4. Molecular Formula: C12H14FNOS
    5. Molecular Weight: 239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107825-27-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 354.9±52.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.242±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 1.26±0.20(Predicted)
    10. CAS DataBase Reference: Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-(CAS DataBase Reference)
    11. NIST Chemistry Reference: Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-(107825-27-4)
    12. EPA Substance Registry System: Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-(107825-27-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 107825-27-4(Hazardous Substances Data)

107825-27-4 Usage

Uses

Used in Pharmaceutical Industry:
Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)is used as a potential drug agent for its demonstrated biological activities. Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-'s unique structural features and its performance in preclinical studies make it a valuable candidate for the development of new therapeutics.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)is utilized for its potential to contribute to the discovery and design of novel pharmaceuticals. Its specific structural elements, including the fluorophenyl and morpholinyl groups, offer avenues for exploration in the synthesis of new compounds with improved pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 107825-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,2 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107825-27:
(8*1)+(7*0)+(6*7)+(5*8)+(4*2)+(3*5)+(2*2)+(1*7)=124
124 % 10 = 4
So 107825-27-4 is a valid CAS Registry Number.

107825-27-4SDS

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 2-(4-fluorophenyl)-1-morpholinoethanethione

1.2 Other means of identification

Product number -
Other names 2-(4-FLUOROPHENYL)-1-(4-MORPHOLINYL)-ETHANETHIONE

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:107825-27-4 SDS

107825-27-4Downstream Products

107825-27-4Relevant articles and documents

Rapid and efficient protocol for Willgerodt–Kindler’s thioacetamides catalyzed by sulfated polyborate

Rekunge, Deelip S.,Khatri, Chetan K.,Chaturbhuj, Ganesh U.

, p. 2091 - 2095 (2017)

Abstract: A simple and efficient method for the synthesis of one-pot, three-component thioacetamides via Willgerodt–Kindler reaction was developed using a sulfated polyborate catalyst. The method described the reaction of ketones, sulfur, and secondary am

Preparation method of phenyl crotonic acid ester compound

-

Paragraph 0030-0032; 0036; 0056-0057, (2021/05/19)

The invention relates to the technical field of organic synthesis, in particular to a preparation method of a phenyl crotonate compound, the preparation method comprises the following steps: S1, carrying out Willgerodt-Kindler reaction on an acetophenone

Optimum Conditions for the Willgerodt-Kindler Reaction 1: Reaction of Substituted Acetophenones. Prediction of Optimum Conditions for New Substrates by Multivariate Correlation

Carlson, Rolf,Lundstedt, Torbjoern,Shabana, Rashad

, p. 534 - 544 (2007/10/02)

Optimum conditions for the synthesis of p-substituted phenyl-acetic acid thiomorpholides by the joint action of elemental sulfur and morpholine on p-substituted acetophenones have been studied with the following substrates: p-methoxy-, p-N,N-dimethylamino

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