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39981-80-1

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39981-80-1 Usage

Description

4-Thiomorpholine acetic acid, ethyl ester is an organic compound derived from thiomorpholine and acetic acid, characterized by its ethyl ester form that facilitates easy handling, manipulation, and transportation. It is recognized for its potential biological activities and versatility in various industrial applications, particularly in the synthesis of pharmaceutical drugs, agrochemicals, and specialty chemicals.

Uses

Used in Pharmaceutical Industry:
4-Thiomorpholine acetic acid, ethyl ester is used as a reagent or intermediate for the synthesis of various pharmaceutical drugs. Its unique chemical structure allows it to be incorporated into the manufacturing processes of a wide range of medicinal compounds, contributing to the development of novel therapeutic agents.
Used in Chemical Industry:
In the chemical industry, 4-Thiomorpholine acetic acid, ethyl ester serves as a key intermediate in the production of specialty chemicals. Its versatility and reactivity make it a valuable component in the synthesis of various organic compounds, enhancing the capabilities of chemical manufacturing processes.
Used in Agrochemical Industry:
4-Thiomorpholine acetic acid, ethyl ester is utilized in the agrochemical sector for the synthesis of various agrochemicals. Its potential applications in this industry include the development of pesticides, herbicides, and other agricultural chemicals, contributing to the enhancement of crop protection and yield optimization.
Used in Research and Development:
4-Thiomorpholine acetic acid, ethyl ester is employed in research and development for the exploration of its potential biological activities. Studies on this compound have been conducted to investigate its medicinal applications, with the aim of discovering new therapeutic agents and expanding the scope of its use in the pharmaceutical field.

Check Digit Verification of cas no

The CAS Registry Mumber 39981-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,8 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39981-80:
(7*3)+(6*9)+(5*9)+(4*8)+(3*1)+(2*8)+(1*0)=171
171 % 10 = 1
So 39981-80-1 is a valid CAS Registry Number.

39981-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-thiomorpholin-4-ylacetate

1.2 Other means of identification

Product number -
Other names ETHYL 2-THIOMORPHOLINOACETATE

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:39981-80-1 SDS

39981-80-1Downstream Products

39981-80-1Relevant articles and documents

Conventional and Microwave-assisted Total Synthesis, Antioxidant Capacity, Biological Activity, and Molecular Docking Studies of New Hybrid Compounds

Demirci, Serpil,Mermer, Arif,Ak, Gokhan,Aksakal, Fatma,Colak, Nesrin,Demirbas, Ahmet,Ayaz, Faik Ahmet,Demirbas, Neslihan

, p. 1785 - 1805 (2017)

Thiomorpholine was converted to the corresponding 1,3,4-oxadiazole (4), arylidenehydrazide (5a, 5b, 5c, 5d, 5e), and 1,2,4-triazole (7a and, 7b) derivatives via the formation of hydrazide (3). Compounds 4 and 7 were next converted to the corresponding Man

Synthesis of novel Schiff bases and azol-β-lactam derivatives starting from morpholine and thiomorpholine and investigation of their antitubercular, antiurease activity, acethylcolinesterase inhibition effect and antioxidant capacity

Cebeci, Y?ld?z Uygun,Bayrak, Hacer,?irin, Yakup

, (2019/04/25)

In this study, new Schiff bases and β-lactam derivatives containing morpholine and thio morpholine nuclei were synthesized. Antimicrobial, antioxidant, antimicrobial and antioxidant properties of all synthesized compounds were investigated and highly effe

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