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5-MORPHOLIN-4-YL-1,3,4-THIADIAZOL-2-AMINE is a heterocyclic chemical compound characterized by the fusion of a morpholinyl group with a 1,3,4-thiadiazol-2-amine structure. 5-MORPHOLIN-4-YL-1,3,4-THIADIAZOL-2-AMINE features a six-membered morpholine ring containing oxygen and nitrogen, attached to a five-membered thiadiazole ring with two nitrogen atoms and one sulfur atom. Its unique chemical structure endows it with a range of potential biological activities, positioning it as a candidate for pharmaceutical development. Further research is essential to fully understand its pharmacological potential and explore its applications within the pharmaceutical industry.

71125-44-5

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71125-44-5 Usage

Uses

Used in Pharmaceutical Industry:
5-MORPHOLIN-4-YL-1,3,4-THIADIAZOL-2-AMINE is used as a potential therapeutic agent for the treatment of various diseases due to its diverse biological activities and unique chemical structure. Its heterocyclic nature may contribute to its interaction with biological targets, offering opportunities for the development of new drugs.
The specific applications and reasons for the use of 5-MORPHOLIN-4-YL-1,3,4-THIADIAZOL-2-AMINE in the pharmaceutical industry are not detailed in the provided materials. However, given its potential biological activities, it may be utilized in the following ways:
As a lead compound in drug discovery for targeting specific diseases or conditions.
For the development of new pharmaceuticals with novel mechanisms of action.
In the synthesis of derivative compounds to enhance pharmacological properties such as potency, selectivity, and bioavailability.
Further research is necessary to determine the exact applications and therapeutic uses of 5-MORPHOLIN-4-YL-1,3,4-THIADIAZOL-2-AMINE, as well as to evaluate its safety and efficacy in clinical settings.

Check Digit Verification of cas no

The CAS Registry Mumber 71125-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,2 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71125-44:
(7*7)+(6*1)+(5*1)+(4*2)+(3*5)+(2*4)+(1*4)=95
95 % 10 = 5
So 71125-44-5 is a valid CAS Registry Number.

71125-44-5SDS

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 5-morpholin-4-yl-1,3,4-thiadiazol-2-amine

1.2 Other means of identification

Product number -
Other names 5-Morpholino-1,3,4-thiadiazol-2-ylamine

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:71125-44-5 SDS

71125-44-5Downstream Products

71125-44-5Relevant academic research and scientific papers

1,3,4-THIADIAZOLES USEFUL FOR THE TREATMENT OF CMV INFECTIONS

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, (2008/06/13)

The present invention presents novel 1,3,4-thiadiazole derivatives of formula I which have useful antiviral activity against herpes virus, cytomegalovirus (CMV).

1,3,4-thiadiazoles useful for the treatment of CMV infections

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, (2008/06/13)

The present invention presents novel 1,3,4-thiadiazole derivatives of formula I which have useful antiviral activity against herpes virus, cytomegalovirus (CMV).

7H-1,3,4-Thiadiazolo-[3,2-a]-pyrimidin-7-one-5-carboxylic compounds

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, (2008/06/13)

Derivatives of 7H-1,3,4-thiadiazolo-[3,2-a]-pyrimidin-7-one-5-carboxylic acid having basic substituents in the 2-position, the alkyl esters and/or pharmaceutically useable salts of these compounds are new substances having immunstimulating properties, being especially valuable for antiinfectious therapy in mammals including man. The new products are prepared by reacting 2-amino-5-(basically substituted)-1,3,4-thiadiazoles with dialkylacetylenedicarboxylates and splitting the ester grouping in the obtained compound if desired and/or forming pharmaceutically acceptable salts.

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