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70156-57-9

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70156-57-9 Usage

Description

2-Phenylthiomorpholin-3-one, a heterocyclic compound with the molecular formula C10H11NOS, features a morpholine ring with a phenylthio group attached. This versatile chemical entity is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as its demonstrated capabilities as an enzyme inhibitor in inflammatory and autoimmune diseases, along with its antiproliferative and antimicrobial properties.

Uses

Used in Pharmaceutical Industry:
2-Phenylthiomorpholin-3-one is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to inhibit enzymes involved in inflammatory and autoimmune diseases. Its unique structure allows for the development of drugs that can modulate biological pathways, offering new treatment options for patients.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Phenylthiomorpholin-3-one serves as a building block in the creation of agrochemicals, contributing to the development of more effective and targeted pesticides and other agricultural products. Its role in this industry is crucial for enhancing crop protection and yield.
Used in Enzyme Inhibition:
2-Phenylthiomorpholin-3-one is utilized as an enzyme inhibitor, particularly for those enzymes that play a role in inflammatory and autoimmune diseases. By inhibiting these enzymes, the compound can help regulate immune responses and reduce inflammation, offering therapeutic benefits in the treatment of such conditions.
Used in Antiproliferative Applications:
2-PHENYLTHIOMORPHOLIN-3-ONE is also used in antiproliferative applications, where it can help control the unregulated cell growth often associated with cancer. Its ability to inhibit cell proliferation makes it a potential candidate for use in cancer research and treatment.
Used in Antimicrobial Applications:
2-Phenylthiomorpholin-3-one has been studied for its antimicrobial properties, making it a useful compound in the development of new antimicrobial agents. Its potential to combat microbial infections positions it as a valuable asset in the ongoing battle against antibiotic resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 70156-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,5 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70156-57:
(7*7)+(6*0)+(5*1)+(4*5)+(3*6)+(2*5)+(1*7)=109
109 % 10 = 9
So 70156-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2S/c12-8-6-13-9(10(14)11-8)7-4-2-1-3-5-7/h1-5,9H,6H2,(H,11,12,14)

70156-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-PHENYLTHIOMORPHOLIN-3-ONE

1.2 Other means of identification

Product number -
Other names 2-phenyl-3-thiomorpholinone

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:70156-57-9 SDS

70156-57-9Relevant articles and documents

Thiomorpholine Derivatives with Hypolipidemic and Antioxidant Activity

Tooulia, Kyriaki-Konstantina,Theodosis-Nobelos, Panagiotis,Rekka, Eleni A.

, p. 629 - 634 (2015/09/15)

A number of thiomorpholine derivatives that are structurally similar to some substituted morpholines possessing antioxidant and hypocholesterolemic activity were synthesized. The new compounds incorporate an antioxidant moiety as the thiomorpholine N-subs

Cyclization of α- and β-alkylthio-substituted amines possessing positively charged carbon at the nitrogen. A new synthetic method for thiazolidines, thiomorpholines and dihydro-1,4-benzothiazines

Ishikawa,Terao,Suzuki,et al.

, p. 438 - 446 (2007/10/02)

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